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Saturday, April 2, 2022

Biotech M&A, despite big expectations, has yet to pick back up: latest deals

 In the business of drug development, deals can be just as important as scientific breakthroughs. Many of today's most influential medicines, from the life-saving cancer treatment Keytruda to the anti-inflammatory agent Humira, might not have become so without mergers and acquisitions.

Over the last few years, pharmaceutical M&A hit record highs as larger companies turned again and again to young biotechs for innovation. Often, these deals focused on cancer, rare diseases and immune system disorders — areas of drug research that were seeing major victories in clinical trials and huge profits for treatments that made it to market.

These deals haven't come cheap, however. Biotech companies have had an easy time raising huge sums of money from private investors and, until recently, the public markets. That funding can make them less receptive to a buyout offer and force would-be acquirers to offer more to lock down deals. Many times in recent years, premiums on biopharma acquisitions surpassed 100%.

While M&A was plentiful in 2018 and 2019, and even held up during a year gripped by the coronavirus pandemic, 2021 was much quieter. In fact, the second quarter hit a five-year low in both the value and number of biopharma transactions. This year, too, has seen only a small amount of activity thus far, though analysts believe a resurgence is likely. Whether this down trend in M&A activity continues, or reverts back to pre-pandemic levels, will have a significant effect on which drug programs get funded and advanced.

BioPharma Dive is tracking these deals below. The database, which shows drugmaker acquisitions that happened since 2018 and were valued at $50 million or more in upfront consideration, will be regularly updated.

Click on an acquiring company to pull up more information, and scroll to the bottom of the page to read how this information was collected and organized. If there's anything we've missed, or any additional information you'd like to see, please reach out and let us know.

Editor's note: If tables or values do not display, please try clearing your browser's cache and reloading the page.

DATABASE
SUMMARY TABLES
ACQUIRER
COMPANY ACQUIRED
DATE OF DEAL
TOTAL CONSIDERATION
PRICE PER SHARE
PREMIUM
Eagle Pharmaceuticals
Acacia Pharma
3/28/22
€95M
€0.90
N/A
Therapeutic focus:
Other
Financial advisors:
William Blair & Company, Greenhill & Co. International, Jefferies International
Legal advisors:
Cooley; NautaDutilh; Sullivan & Cromwell; Eubelius CVBA
Additional consideration:
23 million euros of upfront consideration paid in Eagle Pharma common stock. Eagle also guaranteed 25 million euros of Acacia Pharma debt
AbbVie
Syndesi Therapeutics
3/1/22
$130M
N/A
N/A
Therapeutic focus:
CNS
Financial advisors:
Lazard
Legal advisors:
Cleary Gottlieb Steen & Hamilton; Goodwin Procter; Deloitte Legal, Belgium
Additional consideration:
Conditional milestone payments worth up to $870 million
Biohaven Pharmaceutical
Channel Biosciences
2/25/22
$100M
N/A
N/A
Therapeutic focus:
CNS
Financial advisors:
N/A
Legal advisors:
N/A
Additional consideration:
$65 million of upfront consideration paid in Biohaven common stock. Conditional milestone payments worth up to $1.1 billion
Collegium
Biodelivery Sciences
2/14/22
$604M
$5.60
54%
Therapeutic focus:
Other
Financial advisors:
Jefferies, Moellis & Company
Legal advisors:
Troutman Pepper Hamilton Sanders; Goodwin Procter
UCB
Zogenix
1/19/22
$1,900M
$26.00
66%
Therapeutic focus:
Rare
Financial advisors:
Lazard, Barclays, Bank of America Securities, SVB Leerink
Legal advisors:
Covington & Burling; Latham & Watkins
Additional consideration:
Contingent value rights worth $2 per share
Novartis
Gyroscope
12/22/21
$800M
N/A
N/A
Therapeutic focus:
Other
Financial advisors:
N/A
Legal advisors:
N/A
Additional consideration:
Conditional milestone payments worth up to $700 million
Sanofi
Amunix Pharmaceuticals
12/21/21
$1,000M
N/A
N/A
Therapeutic focus:
Cancer
Financial advisors:
Centerview Partners
Legal advisors:
Weil, Gotshal & Manges; Fenwick & West
Additional consideration:
Conditional milestone payments worth up to $225 million
CSL Ltd
Vifor Pharma
12/14/21
$11,700M
$179.25
19%
Therapeutic focus:
Other
Financial advisors:
Centerview Partners, PJT Partners, Bank of America, Goldman Sachs, Credit Suisse
Legal advisors:
Homburger AG; Simpson Thacher & Bartlett; Allens
Pfizer
Arena Pharmaceuticals
12/13/21
$6,700M
$100.00
100%
Therapeutic focus:
Immune
Financial advisors:
Bank of America, Centerview Partners, Guggenheim Securities, Evercore
Legal advisors:
Ropes & Gray; Arnold & Porter Kaye Scholer; Cooley
Recordati
EUSA Pharma
12/3/21
€750M
N/A
N/A
Therapeutic focus:
Other
Financial advisors:
N/A
Legal advisors:
N/A
Additional consideration:
Aquisition price of 750 million euros reflects enterprise value of EUSA Pharma
Blueprint Medicines
Lengo Therapeutics
11/29/21
$250M
N/A
N/A
Therapeutic focus:
Cancer
Financial advisors:
Goldman Sachs, Centerview Partners
Legal advisors:
Goodwin Procter; Cooley
Additional consideration:
Conditional milestone payments worth up to $215 million
Twist Biosciences
Abveris
11/22/21
$150M
N/A
N/A
Therapeutic focus:
Other
Financial advisors:
Edgemont Partners
Legal advisors:
Nutter, McClennen & Fish
Additional consideration:
Conditional payments worth up to $50 million in cash and Twist common stock
Vifor
Sanifit
11/22/21
€205M
N/A
N/A
Therapeutic focus:
Other
Financial advisors:
N/A
Legal advisors:
N/A
Additional consideration:
Conditional milestone payments worth up to 170 million euros
Novo Nordisk
Dicerna
11/18/21
$3,300M
$38.25
80%
Therapeutic focus:
Other
Financial advisors:
Evercore
Legal advisors:
Davis Polk & Wardwell
Organon
Forendo Pharma
11/11/21
$75M
N/A
N/A
Therapeutic focus:
Other
Financial advisors:
N/A
Legal advisors:
N/A
Additional consideration:
Debt and conditional milestone payments worth up to $879 million
Supernus Pharmaceuticals
Adamas Pharmaceuticals
10/11/21
$400M
$8.10
76%
Therapeutic focus:
CNS
Financial advisors:
Jefferies, Lazard
Legal advisors:
Saul Ewing Arnstein & Lehr; Cooley
Additional consideration:
Contingent value rights worth $1 per share
Pacira Biosciences
Flexion Therapeutics
10/11/21
$425M
$8.50
47%
Therapeutic focus:
CNS
Financial advisors:
J.P. Morgan, Lazard, Goldman Sachs
Legal advisors:
Cooley; Perkins Cole
Additional consideration:
Contingent value right worth $8 per share
Merck & Co.
Acceleron
9/30/21
$11,500M
$180.00
3%
Therapeutic focus:
Rare
Financial advisors:
Credit Suisse, Goldman Sachs, Centerview Partners, J.P. Morgan Securities
Legal advisors:
Covington & Burling; Gibson, Dunn & Crutcher; Ropes & Gray
AstraZeneca
Caelum Biosciences
9/29/21
$150M
N/A
N/A
Therapeutic focus:
Rare
Financial advisors:
N/A
Legal advisors:
N/A
Additional consideration:
Conditional milestone payments worth up to $350 million
Hikma Pharmaceuticals
Custopharm
9/27/21
$375M
N/A
N/A
Therapeutic focus:
Other
Financial advisors:
N/A
Legal advisors:
N/A
Additional consideration:
Conditional milestone payments worth $50 million
Grifols
Biotest
9/17/21
€1,086M
€43.00
23%
Therapeutic focus:
Other
Financial advisors:
Nomura Securities International, UBS Europe
Legal advisors:
Osborne Clarke Spain Germany and UK; Proskauer Rose
Additional consideration:
Grifols to acquire Tiancheng Pharmaceutical Holdings' stake in Biotest, representing 90% of Biotest ordinary shares and 1% of preferred shares.
Sanofi
Kadmon Holdings
9/8/21
$1,900M
$9.50
79%
Therapeutic focus:
Other
Financial advisors:
Cantor Fitzgerald, Moelis & Company
Legal advisors:
Weil, Gotshal & Manges; DLA Piper
Pfizer
Trillium Therapeutics
8/23/21
$2,260M
$18.50
204%
Therapeutic focus:
Cancer
Financial advisors:
Bank of America, Centerview Partners
Legal advisors:
Ropes & Gray; Norton Rose Fulbright Canada; Goodwin Procter; Baker McKenzie
Bayer
Vividion Therapeutics
8/5/21
$1,500M
N/A
N/A
Therapeutic focus:
Cancer
Financial advisors:
Credit Suisse, Centerview Partners
Legal advisors:
Baker McKenzie; Cooley
Additional consideration:
Conditional milestone payments worth up to $500 million
Sanofi
Translate Bio
8/3/21
$3,200M
$38.00
30%
Therapeutic focus:
Other
Financial advisors:
Morgan Stanley, Centerview Partners, Evercore, MTS Health Partners
Legal advisors:
Weil, Gotshal & Manges; Paul, Weiss, Rifkind, Wharton & Garrison
Amgen
TeneoBio
7/27/21
$900M
N/A
N/A
Therapeutic focus:
Cancer
Financial advisors:
Goldman Sachs
Legal advisors:
Latham & Watkins; Gunderson Dettmer Stough Villeneuve Franklin & Hachigian
Additional consideration:
Conditional milestone payments worth up to $1.6 billion
UniQure
Corlieve Therapeutics
6/22/21
€46M
N/A
N/A
Therapeutic focus:
CNS
Financial advisors:
SVB Leerink
Legal advisors:
Morgan Lewis; McDermott, Will & Emery
Additional consideration:
Conditional milestone payments worth up to 204 million euros
MorphoSys
Constellation Pharma
6/2/21
$1,700M
$34.00
68%
Therapeutic focus:
Cancer
Financial advisors:
Goldman Sachs, Centerview Partners
Legal advisors:
Skadden, Arps, Slate, Meagher & Flom; Wachtell, Lipton, Rosen & Katz
Xeris Pharmaceuticals
Strongbridge BioPharma
5/24/21
$267M
$2.72
13%
Therapeutic focus:
Rare
Financial advisors:
SVB Leerink, MTS Health Partners
Legal advisors:
Goodwin Proctor; A&L Goodbody; Skadden, Arthur & Cox
Additional consideration:
Contingent value right worth $1.00 per share
Relay Therapeutics
ZebiAI
4/16/21
$85M
N/A
N/A
Therapeutic focus:
Other
Financial advisors:
N/A
Legal advisors:
N/A
Additional consideration:
Conditional milestone payments worth up to $85 million
Sanofi
Tidal Therapeutics
4/9/21
$160M
N/A
N/A
Therapeutic focus:
Cancer
Financial advisors:
N/A
Legal advisors:
N/A
Additional consideration:
Conditional milestone payments worth up to $310 million
Amgen
Rodeo Therapeutics
3/30/21
$55M
N/A
N/A
Therapeutic focus:
Immune
Financial advisors:
N/A
Legal advisors:
Cooley, Gundersen Dettmer
Additional consideration:
Conditional milestone payments worth up to $666 million
Amgen
Five Prime Therapeutics
3/4/21
$1,900M
$38.00
79%
Therapeutic focus:
Cancer
Financial advisors:
Goldman Sachs, Lazard
Legal advisors:
Sullivan & Cromwell; Cooley
Merck & Co.
Pandion Therapeutics
2/25/21
$1,850M
$60.00
134%
Therapeutic focus:
Immune
Financial advisors:
Credit Suisse, Centerview Partners
Legal advisors:
Covington & Burling; Skadden, Arps, Slate, Meagher & Flom
Beam Therapeutics
Guide Therapeutics
2/23/21
$120M
N/A
N/A
Therapeutic focus:
Other
Financial advisors:
N/A
Legal advisors:
N/A
Additional consideration:
Conditional "technology and product success" milestones worth up to $320 million
Jazz Pharmaceuticals
GW Pharma
2/3/21
$7,200M
$220.00
50%
Therapeutic focus:
Rare
Financial advisors:
Evercore, Guggenheim Securities, Bank of America, J.P. Morgan, Goldman Sachs, Centerview Partners
Legal advisors:
Watchell, Lipton, Rosen & Katz; Macfarlanes; Arthur Cox; Cravath, Swaine & Moore; Slaughter and May
Horizon Pharmaceuticals
Viela Bio
2/1/21
$3,050M
$53.00
53%
Therapeutic focus:
Rare
Financial advisors:
Morgan Stanley, Goldman Sachs
Legal advisors:
Cooley; Mintz, Levin, Cohn, Ferris, Glovsky and Popeo
Sanofi
Kymab
1/11/21
$1,100M
N/A
N/A
Therapeutic focus:
Immune
Financial advisors:
J.P. Morgan
Legal advisors:
Weil, Gotshal & Manges; Goodwin Proctor
Additional consideration:
Conditional milestone payments worth up to $350 million
Chimerix
Oncoceutics
1/8/21
$78M
N/A
N/A
Therapeutic focus:
Cancer
Financial advisors:
Evercore
Legal advisors:
Cooley; Morgan Lewis
Additional consideration:
Conditional milestone payments worth up to $360 million
Angelini Pharma
Arvelle Therapeutics
1/4/21
$610M
N/A
N/A
Therapeutic focus:
CNS
Financial advisors:
Centerview Partners
Legal advisors:
Sidley Austin; NautaDutih; White & Case
Additional consideration:
Conditional milestone payments worth up to $350 milion
Novartis
Cadent Therapeutics
12/17/20
$210M
N/A
N/A
Therapeutic focus:
CNS
Financial advisors:
N/A
Legal advisors:
N/A
Additional consideration:
Conditional milestone payments worth up to $560 million
Eli Lilly
Prevail Therapeutics
12/15/20
$880M
$22.50
80%
Therapeutic focus:
CNS
Financial advisors:
Lazard, Centerview Partners
Legal advisors:
Weil, Gotshal & Manges; Ropes & Gray; Cooley
Additional consideration:
Contingent value right worth $4.00 per share
AstraZeneca
Alexion Pharmaceuticals
12/12/20
$39,000M
$175.00
45%
Therapeutic focus:
Rare
Financial advisors:
Evercore, Centerview Partners, Ondra, Morgan Stanley, J.P. Morgan, Goldman Sachs, Bank of America
Legal advisors:
Freshfields Bruckhaus Deringer; Wachtell, Lipton, Rosen & Katz
Gilead
Myr Pharmaceuticals
12/10/20
$1,200M
N/A
N/A
Therapeutic focus:
Infectious
Financial advisors:
Goldman Sachs, UBS
Legal advisors:
Gibson, Dunn & Crutcher; Mayer Brown; Flick Gocke Schaumburg; Freshfield Bruckhaus Deringer
Additional consideration:
Conditional milestone payments worth up to $360 million
Sumitomo Dainippon
Urovant
11/13/20
$584M
$16.25
N/A
Therapeutic focus:
Other
Financial advisors:
Citi, Lazard
Legal advisors:
O'Melveny & Myers; Jones Day
Merck & Co.
VelosBio
11/5/20
$2,750M
N/A
N/A
Therapeutic focus:
Cancer
Financial advisors:
J.P. Morgan, Centerview Partners
Legal advisors:
Gibson, Dunn & Crutcher; Cooley
Sanofi
Kiadis Pharma
11/2/20
€308M
€5.45
272%
Therapeutic focus:
Cancer
Financial advisors:
PJT Partners, Moelis & Co.
Legal advisors:
NautaDutih, Allen and Overy
Bayer
Asklepios Biopharmaceuticals
10/26/20
$2,000M
N/A
N/A
Therapeutic focus:
Rare
Financial advisors:
Credit Suisse, J.P. Morgan
Legal advisors:
Baker McKenzie; Ropes & Gray
Additional consideration:
Conditional milestone payments worth up to $2 billion
Retrophin
Oprhan Technologies
10/22/20
$90M
N/A
N/A
Therapeutic focus:
Rare
Financial advisors:
Barclays, Cantor Fitzgerald
Legal advisors:
Cooley; Hogan Lovells
Additional consideration:
Conditional milestone payments worth up to $427 million
Endo International
Biospecifics
10/19/20
$540M
$88.50
45%
Therapeutic focus:
Other
Financial advisors:
PJT Partners
Legal advisors:
Skadden, Arps, Slate, Meagher & Flom
Bristol Myers Squibb
Myokardia
10/5/20
$13,100M
$225.00
61%
Therapeutic focus:
Other
Financial advisors:
Gordon Dyal, Centerview Partners, Guggenheim Securities
Legal advisors:
Kirkland & Ellis; Goodwin Procter
Covis Group
AMAG Pharma
10/1/20
$647M
$13.75
46%
Therapeutic focus:
Other
Financial advisors:
Goldman Sachs
Legal advisors:
Goodwin Procter; Paul, Weiss, Rifkind, Wharton and Garrison
Roche
Inflazome
9/21/20
€380M
N/A
N/A
Therapeutic focus:
Immune
Financial advisors:
Lazard
Legal advisors:
Goodwin Procter; Byrne Wallace
Additional consideration:
Unspecified conditional milestone payments
Gilead
Immunomedics
9/13/20
$21,000M
$88.00
108%
Therapeutic focus:
Cancer
Financial advisors:
Lazard, Morgan Stanley, Centerview Partners, Bank of America, Cowen
Legal advisors:
Davis Polk & Wardwell; Watchell, Lipton, Rosen & Katz
Nestle
Aimmune Therapeutics
8/31/20
$2,160M
$34.50
174%
Therapeutic focus:
Other
Financial advisors:
J.P. Morgan, Lazard
Legal advisors:
Latham & Watkins
Ionis Pharmaceuticals
Akcea Therapeutics
8/31/20
$500M
$18.15
60%
Therapeutic focus:
Rare
Financial advisors:
Goldman Sachs, Stifel, Nicolaus & Company, Cowen
Legal advisors:
Skadden, Arps, Slate, Meagher & Flom; Ropes & Gray
Acadia Pharmaceuticals
CerSci Therapeutics
8/25/20
$53M
N/A
N/A
Therapeutic focus:
Other
Financial advisors:
Bank of America, Evercore
Legal advisors:
Paul Hastings; Skadden, Arps, Slate, Meagher & Flom
Additional consideration:
Conditional milestone payments worth up to $887 million
Johnson & Johnson
Momenta Pharmaceuticals
8/19/20
$6,500M
$52.50
70%
Therapeutic focus:
Immune
Financial advisors:
Goldman Sachs, Centerview Partners
Legal advisors:
Latham & Watkins; Skadden, Arps, Slate, Meagher & Flom
Sanofi
Principia Biopharma
8/17/20
$3,680M
$100.00
10%
Therapeutic focus:
Immune
Financial advisors:
Evercore, Centerview Partners, Bank of America
Legal advisors:
Weil, Gotshal & Manges; Cooley
Bayer
KaNDy Therapeutics
8/11/20
$425M
N/A
N/A
Therapeutic focus:
Other
Financial advisors:
Morgan Stanley, Goldman Sachs
Legal advisors:
Linklaters; Goodwin Procter
Additional consideration:
Conditional milestone payments worth up to $450 million
Ligand Pharmaceuticals
Pfenex
8/10/20
$438M
$12.00
57%
Therapeutic focus:
Other
Financial advisors:
William Blair, Barclays
Legal advisors:
Wilson Sonsini Goodrich & Rosati; Latham & Watkins
Additional consideration:
Contingent value right worth $2.00 per share
Novo Nordisk
Corvidia Therapeutics
6/11/20
$725M
N/A
N/A
Therapeutic focus:
Immune
Financial advisors:
J.P. Morgan
Legal advisors:
Davis Polk & Wardwell; Goodwin Procter
Additional consideration:
Conditional milestone payments worth up to $1.375 billion
UCB
Engage Therapeutics
6/5/20
$125M
N/A
N/A
Therapeutic focus:
Rare
Financial advisors:
Lazard, BMO Capital Markets
Legal advisors:
Covington & Burling; Morgan, Lewis & Brockius
Additional consideration:
Conditional milestone payments worth up to $145 million
Alexion Pharmaceuticals
Portola Pharmaceuticals
5/5/20
$1,440M
$18.00
132%
Therapeutic focus:
Other
Financial advisors:
RBC Capital Markets, Centerview Partners
Legal advisors:
Cooley
Menarini Group
Stemline Therapeutics
5/4/20
$677M
$11.50
163%
Therapeutic focus:
Cancer
Financial advisors:
Goldman, PJT Partners, Bank of America
Legal advisors:
Fried, Frank, Harris, Shriver & Jacobson; Skadden, Arps, Slate, Meagher & Flom; Alston & Bird
Additional consideration:
Contingent value right worth $1.00 per share
Gilead
Forty Seven
3/2/20
$4,900M
$95.50
81%
Therapeutic focus:
Cancer
Financial advisors:
Citi, J.P. Morgan, Centerview Partners
Legal advisors:
Skadden, Arps, Slate, Meagher & Flom; Cooley
BioNTech
Neon Therapeutics
1/16/20
$67M
$2.18
77%
Therapeutic focus:
Cancer
Financial advisors:
Ondra Partners
Legal advisors:
Covington & Burling; Goodwin Procter
Eli Lilly
Dermira
1/10/20
$1,100M
$18.75
2%
Therapeutic focus:
Immune
Financial advisors:
Evercore, Citi, SVB Leerink
Legal advisors:
Weil, Gotshal & Manges; Fenwick & West
Sanofi
Synthorx
12/9/19
$2,500M
$68.00
172%
Therapeutic focus:
Cancer
Financial advisors:
Morgan Stanley, Centerview Partners
Legal advisors:
Weill, Gotshal & Manges; Cooley
Merck & Co.
ArQule
12/9/19
$2,700M
$20.00
107%
Therapeutic focus:
Cancer
Financial advisors:
Bank of America, Centerview Partners
Legal advisors:
Covington & Burling; Skadden, Arps, Slate, Meagher & Flom
Astellas Pharma
Audentes Therapeutics
12/2/19
$3,000M
$60.00
110%
Therapeutic focus:
Rare
Financial advisors:
Morgan Stanley, Centerview Partners
Legal advisors:
Covington & Burling; Fenwick & West
Novartis
The Medicines Co.
11/24/19
$9,700M
$85.00
24%
Therapeutic focus:
Other
Financial advisors:
Goldman Sachs, J.P. Morgan
Legal advisors:
Paul, Weiss, Rifkind, Wharton & Garrison
Alkermes
Rodin Therapeutics
11/18/19
$100M
N/A
N/A
Therapeutic focus:
CNS
Financial advisors:
N/A
Legal advisors:
WilmerHale; Goodwin Procter
Additional consideration:
Conditional milestone payments worth up to $850 million
Roche
Promedior
11/15/19
$390M
N/A
N/A
Therapeutic focus:
Other
Financial advisors:
N/A
Legal advisors:
Goodwin
Additional consideration:
Conditional milestone payments worth up to $1 billion
Alexion Pharmaceuticals
Achillion Pharmaceuticals
10/16/19
$930M
$6.30
73%
Therapeutic focus:
Immune
Financial advisors:
Centerview Partners
Legal advisors:
Skadden, Arps, Slate, Meagher & Flom
Additional consideration:
Contingent value right worth $2.00 per share
UCB
Ra Pharma
10/10/19
$2,100M
$48.00
111%
Therapeutic focus:
Rare
Financial advisors:
Bank of America, Lazard, Centerview Partners
Legal advisors:
Covington & Burling; Latham & Watkins
Swedish Orphan Biovitrum (Sobi)
Dova Pharmaceuticals
9/30/19
$868M
$27.50
36%
Therapeutic focus:
Other
Financial advisors:
Morgan Stanley
Legal advisors:
Cravath, Swaine & Moore; Mannheimer Swartling Advokatbyrå
Additional consideration:
Contingent value right worth $1.50 per share
Lundbeck
Alder Biopharmaceutical
9/16/19
$2,000M
$18.00
79%
Therapeutic focus:
CNS
Financial advisors:
MTS Health Partners, PJT Partners, Centerview Partners
Legal advisors:
Skadden, Arps, Slate, Meagher & Flom; Baker McKenzie; Cooley
Additional consideration:
Contingent value right worth $2.00 per share
Vertex
Semma Therapeutics
9/3/19
$950M
N/A
N/A
Therapeutic focus:
Other
Financial advisors:
N/A
Legal advisors:
N/A
Amgen
Otezla
8/26/19
$13,400M
N/A
N/A
Therapeutic focus:
Immune
Financial advisors:
Dyal, Goldman Sachs
Legal advisors:
Sullivan & Cromwell
Zogenix
Modis Therapeutics
8/26/19
$250M
N/A
N/A
Therapeutic focus:
Rare
Financial advisors:
SVB Leerink
Legal advisors:
Lantham & Watkins; Fenwick & West
Additional consideration:
Conditional milestone paymnets worth up to $150 million
Bayer
Bluerock Therapeutics
8/8/19
$240M
N/A
N/A
Therapeutic focus:
CNS
Financial advisors:
N/A
Legal advisors:
Orrick
Additional consideration:
Conditional milestone payments worth up to $360 million
AbbVie
Allergan
6/25/19
$63,000M
$120.30
45%
Therapeutic focus:
Other
Financial advisors:
Morgan Stanley, PJT Partners, J.P. Morgan
Legal advisors:
Kirkland & Ellis; McCann FitzGerald; Wachtell, Lipton, Rosen & Katz and Arthur Cox
Pfizer
Array Biopharma
6/17/19
$11,400M
$48.00
62%
Therapeutic focus:
Cancer
Financial advisors:
Guggenheim Securities, Morgan Stanley, Centerview Partners
Legal advisors:
Wachtell, Lipton, Rosen & Katz; Skadden, Arps, Slate, Meagher & Flom
Vertex
Exonics
6/6/19
$245M
N/A
N/A
Therapeutic focus:
CNS
Financial advisors:
N/A
Legal advisors:
N/A
Additional consideration:
Conditional milestone payments worth approximately $755 million
Merck & Co.
Peloton Therapeutics
5/21/19
$1,050M
N/A
N/A
Therapeutic focus:
Cancer
Financial advisors:
Credit Suisse, Centerview Partners
Legal advisors:
Covington & Burling; Wilson, Sonsini, Goodrich & Rosati
Additional consideration:
Conditional milestone payments worth up to $1.15 billion
Pfizer
Therachon Holding
5/8/19
$340M
N/A
N/A
Therapeutic focus:
Rare
Financial advisors:
Goldman Sachs
Legal advisors:
Cooley; Homburger; Arnold & Porter; Lenz & Staehelin
Additional consideration:
Conditional milestone payments worth up to $470 million
Novartis
Xiidra
5/8/19
$3,400M
N/A
N/A
Therapeutic focus:
Other
Financial advisors:
Evercore
Legal advisors:
Davis, Polk & Wardwell
Additional consideration:
Conditional milestone payments worth up to $1.9 billion
Lundbeck
Abide Therapeutics
5/6/19
$250M
N/A
N/A
Therapeutic focus:
CNS
Financial advisors:
Credit Suisse, Bank of America
Legal advisors:
Baker McKenzie; Goodwin Proctor
Additional consideration:
Conditional milestone payments of worth to $150 million
Novartis
IFM Tre
4/1/19
$310M
N/A
N/A
Therapeutic focus:
Immune
Financial advisors:
N/A
Legal advisors:
Hogan Lovells
Additional consideration:
Conditional milestone payments of worth to $1.265 billion
Biogen
Nightstar Therapeutics
3/4/19
$800M
$25.50
68%
Therapeutic focus:
Rare
Financial advisors:
Goldman Sachs, Centerview Partners
Legal advisors:
Ropes & Gray; Skadden, Arps, Slate, Meagher & Flom
Sarepta Therapeutics
Myonexus Therapeutics
2/27/19
$165M
N/A
N/A
Therapeutic focus:
CNS
Financial advisors:
William Blair
Legal advisors:
Thompson Hine; Fenwick & West
Roche
Spark Therapeutics
2/25/19
$4,800M
$114.50
122%
Therapeutic focus:
Rare
Financial advisors:
Citi, Centerview Partners, Cowen
Legal advisors:
Davis Polk & Wardwell; Goodwin Proctor
Ipsen
Clementia Pharmaceuticals
2/25/19
$1,040M
$25.00
67%
Therapeutic focus:
Rare
Financial advisors:
Centerview Partners, Morgan Stanley
Legal advisors:
Goodwin Proctor; Davies, Ward, Phillips & Vineberg; Davies; Skadden, Arps, Slate, Meagher & Flom; Stikeman Elliott
Additional consideration:
Contingent value right worth $6.00 per share
Merck & Co.
Immune Design
2/21/19
$300M
$5.85
312%
Therapeutic focus:
Cancer
Financial advisors:
Credit Suisse, Lazard
Legal advisors:
Gibson, Dunn & Crutcher; Cooley
Eli Lilly
Loxo Oncology
1/7/19
$8,000M
$235.00
68%
Therapeutic focus:
Cancer
Financial advisors:
Deustche Bank, Goldman Sachs
Legal advisors:
Weil, Gotshal & Manges; Fenwick & West
Bristol Myers Squibb
Celgene
1/3/19
$74,000M
$102.43
54%
Therapeutic focus:
Cancer
Financial advisors:
Morgan Stanley, Citi, Evercore, Dyal, J.P. Morgan
Legal advisors:
Kirkland & Ellis; Wachtell, Lipton, Rosen & Katz
Additional consideration:
Contingent value right worth $9.00 per share (terminated)
GlaxoSmithKline
Tesaro
12/3/18
$5,100M
$75.00
62%
Therapeutic focus:
Cancer
Financial advisors:
PJT Parners, Bank of America, Citi, Centerview Partners
Legal advisors:
Shearman & Sterling; Slaughter and May; Hogan Lovells; Ropes & Gray
Roche
Jecure Therapeutics
11/27/18
CHF150M
N/A
N/A
Therapeutic focus:
Other
Financial advisors:
N/A
Legal advisors:
N/A
Novartis
Endocyte
10/18/18
$2,100M
$24.00
54%
Therapeutic focus:
Cancer
Financial advisors:
Centerview Partners, Jefferies
Legal advisors:
Faegre Baker Daniels
Roche
Tusk Therapeutics
9/27/18
€70M
N/A
N/A
Therapeutic focus:
Cancer
Financial advisors:
N/A
Legal advisors:
N/A
Additional consideration:
Conditional milestone payments worth up to 585 million euros
Alexion Pharmaceuticals
Syntimmune
9/26/18
$400M
N/A
N/A
Therapeutic focus:
Immune
Financial advisors:
N/A
Legal advisors:
Foley Hoag; Goodwin Proctor; Sullivan & Cromwell
Additional consideration:
Conditional milestone payments worth up to $800 million
Amicus Therapeutics
Celenex
9/20/18
$100M
N/A
N/A
Therapeutic focus:
Rare
Financial advisors:
RBC
Legal advisors:
Skadden, Arps, Slate, Meagher & Flom; Fenwick & West
Additional consideration:
Conditional milestone payments worth up to $352 million
Boehringer Ingelheim
ViraTherapeutics
9/13/18
$210M
N/A
N/A
Therapeutic focus:
Cancer
Financial advisors:
N/A
Legal advisors:
Gleiss Lutz
Additional consideration:
The total transaction value is based on an option and share purchase agreement signed in August 2016
Emergent Biosolutions
Adapt Pharma
8/28/18
$635M
N/A
N/A
Therapeutic focus:
Other
Financial advisors:
Morgan Stanley, Bank of America
Legal advisors:
Covington & Burling; Mayer Brown
Additional consideration:
Conditional milestone payments worth up to $100 million
Sangamo Therapeutics
TxCell
7/23/18
$80M
$2.99
177%
Therapeutic focus:
Immune
Financial advisors:
N/A
Legal advisors:
N/A
Otsuka
Visterra
7/11/18
$430M
N/A
N/A
Therapeutic focus:
Other
Financial advisors:
N/A
Legal advisors:
N/A
Akebia Therapeutics
Keryx Biopharmaceuticals
6/28/18
$528M
N/A
N/A
Therapeutic focus:
Other
Financial advisors:
MTS Health, Evercore, J.P. Morgan Perella Weinberg Partners
Legal advisors:
Lantham & Watkins; Goodwin Proctor
Eli Lilly
AurKa Pharma
5/14/18
$110M
N/A
N/A
Therapeutic focus:
Cancer
Financial advisors:
Baird
Legal advisors:
N/A
Eli Lilly
Armo Biosciences
5/10/18
$1,600M
$50.00
68%
Therapeutic focus:
Cancer
Financial advisors:
Credit Suisse, Centerview Partners, Jefferies
Legal advisors:
Wachtell, Lipton, Rosen & Katz; Gunderson Dettmer
Takeda
Shire
5/7/18
$62,000M
$30.33
27%
Therapeutic focus:
Rare
Financial advisors:
Evercore, JP Morgan, Nomura, Goldman Sachs, Citi, Morgan Stanley
Legal advisors:
Linklaters; Nishimura & Asahi; Ogier; Slaughter and May; Davis, Polk & Wardwell; Nagashima Ohno & Tsunematsu; Mourant Ozannes
Johnson & Johnson
BeneVir Biopharm
5/2/18
$140M
N/A
N/A
Therapeutic focus:
Cancer
Financial advisors:
N/A
Legal advisors:
N/A
United Therapeutics
SteadyMed
4/30/18
$141M
$4.46
68%
Therapeutic focus:
Rare
Financial advisors:
Wedbush PacGrow
Legal advisors:
Gibson, Dunn & Crutcher; Herzog, Fox & Neeman; Cooley; Yigal Arnon & Co.
Additional consideration:
Conditional milestone payment worth $2.63 per share, or a total of $75 million
Alexion Pharmaceuticals
Wilson Therapeutics
4/11/18
$855M
$28.00
N/A
Therapeutic focus:
Rare
Financial advisors:
Bank of America, Deutsche Bank, DNB Markets, Lazard
Legal advisors:
Advokatfirman Cederquist; Ropes & Gray; Vinge
Novartis
AveXis
4/9/18
$8,700M
$218.00
88%
Therapeutic focus:
CNS
Financial advisors:
Goldman Sachs, Centerview Partners, Dyal
Legal advisors:
Cravath, Swaine and Moore; Cooley
Merck & Co.
Viralytics
2/21/18
$394M
$1.37
185%
Therapeutic focus:
Cancer
Financial advisors:
Credit Suisse, Lazard
Legal advisors:
Baker & McKenzie; McCullough Robertson
SeaGen
Cascadian Therapeutics
1/31/18
$614M
$10.00
69%
Therapeutic focus:
Cancer
Financial advisors:
Leerink Partners, Barclays, J.P. Morgan Perella Weinberg Partners
Legal advisors:
Sullivan & Cromwell; Reed Smith; Goodwin Procter
Sanofi
Ablynx
1/29/18
$4,800M
$56.00
21%
Therapeutic focus:
Rare
Financial advisors:
Lazard, J.P. Morgan, Morgan Stanley
Legal advisors:
Weil, Gotshal & Manges; NautaDutilh; Eubelius CVBA; Goodwin Procter; Linklaters
Sanofi
Bioverativ
1/22/18
$11,600M
$105.00
64%
Therapeutic focus:
Rare
Financial advisors:
Lazard, Guggenheim Securities, J.P. Morgan
Legal advisors:
Weil, Gotshal & Manges; Paul, Weiss, Rifkind, Wharton & Garrison
Celgene
Juno Therapeutics
1/22/18
$9,000M
$87.00
29%
Therapeutic focus:
Cancer
Financial advisors:
J.P. Morgan, Morgan Stanley
Legal advisors:
Proskauer Rose; Hogan Lovells; Skadden, Arps, Slate, Meagher and Flom
Takeda
TiGenix
1/4/18
€520M
€1.78
82%
Therapeutic focus:
Other
Financial advisors:
Centerview Partners, Cowen & Co.
Legal advisors:
Osborne Clarke CVBA; Davis, Polk & Wardwell; DLA Piper
*Premiums are calculated from the closing price of the acquired company's shares on the previous trading day.

Methodology

For this story, BioPharma Dive looked only at companies developing human medicines. The mergers and acquisitions included in the database are limited by certain criteria, namely that they must be for an entire company — not for product licensings, options to acquire or for partial equity stakes.

Two exceptions: Amgen's $13.4 billion acquisition of the psoriasis medicine Otezla and Novartis' $3.4 billion acquisition of the dry eye drug Xiidra, which are included for their notable size and importance to the acquirer.

Additionally, the database is limited to deals valued at a minimum of $50 million upfront. Total consideration can reflect both cash and equity offered upfront in exchange for the acquired company’s shares, but deals in which the upfront payment was not specified, or was less than $50 million, were not included.

Premiums were calculated using the acquired company's share price at the previous trading day's close

Only one therapeutic category is counted for each acquired company. For those with multiple focuses, the chosen therapeutic area is based on lead asset or, lacking one that's distinctly identified, the company is classified under "other."

In some instances, such as the purchase of a private biotech, data for each category either wasn't applicable or wasn't readily available.

https://www.biopharmadive.com/news/biotech-pharma-deals-merger-acquisitions-tracker/604262/

5 FDA decisions to watch in the second quarter

 The first quarter of 2022 was one to forget for the biotech industry.

A public market downturn that began last year accelerated, sending the stock values of many biotech companies spiraling lower. The pace of drugmaker initial public offerings, which set a record in 2021, slowed to a trickle, making the path to Wall Street harder for emerging startups. Biotechs tightened their purse strings, leading to a string of restructurings

Still, there were a few bright spots. The Food and Drug Administration approved a first-of-its-kind cancer immunotherapy, while a pioneering gene editing treatment continued to show promise and a major acquisition closed, calming concerns of greater regulatory scrutiny on buyout deals. 

Several key FDA decisions lie ahead in the second quarter and each, if positive, may help the sector regain its momentum. Here are five to watch: 

Bluebird bio's beti-cel in beta thalassemia and eli-cel in CALD  

FDA advisory committee meetings are important moments for drugmakers as their outcomes can have a significant impact on a prospective medicine's approval chances. A two-day gathering in June is even more important for Bluebird, which could run out of money if the FDA doesn't approve two gene therapies a group of experts are set to review. 

The gene therapies, known as beti-cel and eli-cel, would be just the third and fourth gene therapies for inherited diseases to reach market in the U.S. They would represent significant medical advances for patients with the blood disease beta thalassemia and the childhood brain disorder cerebral adrenoleukodystrophy. 

Approvals also would lead the FDA to award the company with two priority review vouchers that can speed up drug reviews and be sold to other companies. 

Bluebird has said those vouchers are critical to its financial future. In March, the company's top financial executive resigned amid a cash crunch that could leave the company insolvent within a year. Selling the vouchers could extend its runway and give Bluebird the chance to rebound. 

However, Bluebird needs the blessing of the FDA and its advisers first, neither of which are a given. Both programs have been slowed in the past due to safety concerns and testing of eli-cel is on hold after a clinical trial participant developed a type of bone marrow cancer. The FDA extended its review of both drugs earlier this year. 

The two-day advisory panel will take place on June 9 and June 10. The FDA will decide whether to approve beti-cel by Aug. 19 and eli-cel by Sept. 16. 

Bristol Myers Squibb's mavacamten in hypertrophic cardiomyopathy 

Bristol Myers Squibb has been largely absent from major dealmaking since absorbing Celgene in a merger three years ago. However, the one time the pharma company did spring for a deal was in October 2020, when it paid $13 billion to buy MyoKardia and a heart drug known as mavacamten. 

Bristol Myers was willing to pay that high price on optimism that mavacamten could become a top seller. On a conference call in February, CEO Giovanni Caforio pointed to the drug, which treats a typically inherited heart condition known as hypertrophic cardiomyopathy, as one of three emerging treatments in its pipeline with "at least $4 billion in revenue potential." Hitting those numbers will be key for Bristol Myers, as some of its most lucrative products will lose patent protection later this decade. 

Still, commercial success is no guarantee. Many patients with hypertrophic cardiomyopathy don't have symptoms, and other medications and surgical options are available. Competition could be looming in the form of a similar drug from Cytokinetics that's in late-stage testing. On the February call, some analysts also questioned Bristol Myers' projections, which rely heavily on a sharp increase in diagnosis rates.

The FDA in November extended its review of mavacamten to evaluate a proposed post-approval patient monitoring plan, the details of which Bristol Myers hasn't shared. Its decision deadline is April 28. 

Amylyx Pharmaceuticals' AMX0035 in amyotrophic lateral sclerosis  

The FDA is set to issue a verdict by June 29 on what could become the first new ALS drug to reach the U.S. market in five years.

ALS, better known to some as amyotrophic lateral sclerosis or Lou Gehrig's disease, is a progressive and fatal disorder hallmarked by the breakdown of nerve cells and the deterioration of essential functions like walking, eating and breathing. Patients with the disease typically live just two to five years after being diagnosed. To date, the FDA has cleared only two treatments specifically for ALS, each with limited effects on function and survival.

Amylyx Pharmaceuticals, a small drug company based in Cambridge, Massachusetts, believes it has another option in a pairing of chemicals named AMX0035. In a study of about 140 patients, Amylyx said those who received its medicine declined significantly slower compared to those on a placebo, as measured by a rating scale used to evaluate day-to-day functions in ALS patients. Amylyx also said that further analyses from an extension phase of the study found a benefit on survival.

The company, patient advocates and some doctors believe these outcomes offer enough evidence to approve AMX0035. The FDA has shown interest in the drug as well, allowing Amylyx to submit it while running another, larger study to confirm the results seen so far. However, the agency also has reservations about the way Amylyx designed its key study and the ways in which data were analyzed. Such concerns were on display during a meeting this week, in which neuroscience and drug development experts advised the FDA against approving AMX0035 in a narrow vote.

That vote puts the agency in a difficult position. ALS patients and advocacy groups have campaigned for the approval of more treatments, including Amylyx's, noting the limited options currently available as well as the devastating and fatal nature of their disease. The FDA has met with advocates and said it's listening to them, but with the crux of Amylyx's approval application in doubt, regulators could hold off green-lighting the company's drug until that larger study produces full results in 2024.

Bristol Myers' Breyanzi in early lymphoma

By late June, the FDA will decide whether to approve Bristol Myers' CAR-T cell therapy Breyanzi for earlier treatment of a common form of lymphoma.

To date, the complex cancer treatments have only been cleared for use after patients have run out of other options, limiting their reach and commercial potential. However, last year Bristol Myers and Gilead presented clinical trial data showing their respective CAR-T therapies — Breyanzi and Yescarta — outperformed standard "second-line" treatment, a combination of chemotherapy and stem cell transplant. 

The results were a major proof point for CAR-T, which had reached market in the U.S. based on smaller studies without control arms. They were also validation for Bristol Myers and Gilead, both of which spent billions of dollars to acquire the products. 

Gilead is likely to beat Bristol Myers to an approval, with an FDA decision expected imminently for Yescarta in second-line treatment. Yescarta has also been approved for longer, with an additional clearance for another lymphoma type. 

However, approvals in second-line lymphoma could also draw renewed attention to the cost and manufacturing issues of CAR-T treatment. Bristol Myers priced Breyanzi at $410,000, while Yescarta has a list price of $373,000. Both companies require several weeks to produce the personalized treatments, a challenge that may grow more difficult if a broader group of patients are eligible. 

TG Therapeutics' ublituximab and Ukoniq in two types of lymphoma

Over the past year, the FDA office in charge of reviewing new cancer medicines has revisited its approach to accelerated approvals, most notably convening a meeting of outside experts last spring to review six previously granted OKs. 

Agency officials have penned opinion pieces signaling tougher standards. FDA pressure has also led a number of companies to withdraw accelerated approval applications. Some companies have even pulled previously cleared drug indications after they were unable to confirm benefits observed in earlier testing. 

The FDA's scrutiny appears to be turning next to a class of cancer medicines known as PI3K inhibitors, several of which are already on the market. In late April, the agency will again gather its panel of advisers to review whether randomized trial data is needed to appropriately support their use. 

The group will also discuss an application by TG Therapeutics for accelerated approval of a combination drug regimen containing its marketed PI3K blocker Ukoniq. Previously, the FDA had announced an investigation into a possible increased risk of death with the medicine. 

The agency has set a target decision date of June 25 for TG's treatment combination. 

Already, the FDA's focus on PI3K inhibitors appears to have had an effect. In January, Gilead said it would withdraw two indications for its drug Zydelig after having difficulty enrolling patients in confirmatory studies. In addition, the agency told MEI Pharma and partner Kyowa Kirin this month that they would need to gather more data for their experimental PI3K inhibitor before seeking approval. 

https://www.biopharmadive.com/news/5-fda-approval-decisions-second-quarter-2022/621342/

NIH begins clinical trial evaluating second COVID-19 booster shots in adults

 Adults interested in joining this study should visit clinicaltrials.gov and search identifier NCT05289037 for a list of sites and contacts.

A Phase 2 clinical trial evaluating various additional COVID-19 booster shots has begun enrolling adult participants in the United States. The trial aims to understand if different vaccine regimens—prototype and variant vaccines alone and in combinations—can broaden immune responses in adults who already have received a primary vaccination series and a first booster shot. The study, known as the COVID-19 Variant Immunologic Landscape (COVAIL) trial, is sponsored by the National Institute of Allergy and Infectious Diseases (NIAID), part of the National Institutes of Health.

“We are looking beyond the Omicron variant to determine the best strategy to protect against future variants,” said NIAID Director Anthony S. Fauci, M.D. “This trial will help us understand if we can use prototype and variant vaccines alone or together to shift immune responses to cover existing and emerging COVID-19 variants.”

Despite waning protection against infection and mild illness during the Omicron wave, COVID-19 vaccines available in the United States so far have maintained durable protection against severe COVID-19. However, NIAID is preparing for the possibility of future variants evading protection against currently available COVID-19 vaccines.

COVID-19 vaccine manufacturers can adjust prototype vaccines to target specific variants, a process similar to how manufacturers update seasonal influenza vaccines every year to target circulating strains. However, predicting if, when and where new COVID-19 variants will emerge and how they will affect the population, remains challenging. Studies(link is external) indicate that Omicron has a combination of mutations that make it substantially different from prior SARS-CoV-2 variants. Should a new variant emerge that more closely resembles ancestral SARS-CoV-2 or, for example, the Delta variant, an Omicron-specific vaccine may not offer substantial protection. An individual’s response to booster shots may also be impacted by their history of prior infection and vaccination, or both, and what type of COVID-19 vaccines they received.

Vaccine manufacturers have previously studied some variant vaccine candidates and are currently conducting clinical trials of Omicron-specific vaccines. The COVAIL trial will gather data on the immune responses induced by prototype vaccines and variant vaccine candidates—including bivalent vaccines, which target two SARS-CoV-2 variants—to inform booster shot recommendations.

Nadine Rouphael, M.D., director of the Hope Clinic at the Emory Vaccine Center in Atlanta, and Angela Branche, M.D., associate professor of medicine at the University of Rochester Medical Center in New York, are leading the trial. Site investigators at 24 clinics are enrolling 600 participants 18 years and older who already have received a primary COVID-19 vaccination series and booster shot. Participants are randomly assigned to one of six vaccine regimens:

  1. One 50-microgram (mcg) injection of the mRNA-1273 (Spikevax) prototype vaccine, which is the same vaccine currently authorized in the United States as a booster shot for adults
  2. One 50-mcg injection consisting of mRNA-1273.351 (an investigational vaccine targeting the Beta variant) and mRNA-1273.529 (an investigational vaccine targeting the Omicron variant)
  3. Two vaccinations administered two months apart: each vaccination is one 50-mcg injection containing both mRNA-1273.351 and mRNA-1273.529
  4. One 50-mcg injection consisting of mRNA-1273.617.2 (an investigational vaccine targeting the Delta variant) and mRNA-1273.529
  5. One 50-mcg injection of mRNA-1273.529
  6. One 50-mcg injection consisting of mRNA-1273 (Spikevax) and mRNA-1273.529

The first stage of this trial is being conducted in collaboration with Moderna, Inc., based in Cambridge, Massachusetts, and Moderna is manufacturing the study vaccines that will be administered. The trial will be adapted to enroll more participants to evaluate additional vaccine platforms and variant vaccines from other manufacturers as needed to further inform public health decisions. Participants will be monitored for symptoms and adverse events following vaccination and will be asked to return to the clinic during set times over the course of 12-14 months to provide blood samples. Investigators will evaluate the samples in the laboratory to measure and characterize immune responses to SARS-CoV-2 strains. Investigators aim to have initial findings available by August 2022.

The study is being conducted in collaboration with academic medical centers across the U.S., NIAID’s Infectious Diseases Clinical Research Consortium (IDCRC) and the NIAID SARS-CoV-2 Assessment of Viral Evolution (SAVE) Program. For more information about the trial, including specific site locations, and for details on how to participate, please visit clinicaltrials.gov and search identifier NCT05289037. The trial is funded through a contract to Frederick National Laboratory for Cancer Research, operated by Leidos Biomedical Research (75N91019D00024) in Frederick, Maryland. The IDCRC’s protocol development work is supported by cooperative agreement UM1AI148684.

NIAID conducts and supports research—at NIH, throughout the United States, and worldwide—to study the causes of infectious and immune-mediated diseases, and to develop better means of preventing, diagnosing and treating these illnesses. News releases, fact sheets and other NIAID-related materials are available on the NIAID website.

About the National Institutes of Health (NIH): NIH, the nation's medical research agency, includes 27 Institutes and Centers and is a component of the U.S. Department of Health and Human Services. NIH is the primary federal agency conducting and supporting basic, clinical, and translational medical research, and is investigating the causes, treatments, and cures for both common and rare diseases. For more information about NIH and its programs, visit www.nih.gov.

https://www.nih.gov/news-events/news-releases/nih-begins-clinical-trial-evaluating-second-covid-19-booster-shots-adults

Pregnancy increases chances of breakthrough COVID

 A new study released Thursday found that those who are pregnant and vaccinated against COVID-19 are twice as likely to get a breakthrough case of the virus than those who aren't pregnant.

Researchers from the Wisconsin-based company Epic said they analyzed the medical records of about 14 million patients that were stored in Cosmos, a HIPAA-defined data set of more than 140 million people from 960 hospitals and 20,814 clinics that serve patients in all 50 states.

According to the study, researchers homed in on what comorbidities could increase a patient's chances of getting a breakthrough COVID-19 case while vaccinated.

They found that pregnant individuals were 1.91 times more likely to get COVID while vaccinated. They also found that those with organ transplants were 1.83 times more likely to get COVID-19, and those with immune deficiency were 1.63 times more likely to get breakthrough COVID.

https://www.wcpo.com/news/national/coronavirus/study-finds-pregnancy-increases-chances-of-breakthrough-covid

NYC to release 6M free at-home COVID tests as cases rise due to BA.2

 Amid rising coronavirus (COVID-19) cases in New York City, Mayor Eric Adams said the city will distribute 6.3 million free at-home COVID tests, and is again recommending masks be worn by all people when inside public spaces.

The uptick in COVID cases is due to the BA.2 variant, said Dr. Ashwin Vasan, commissioner of the New York City Department of Health and Mental Hygiene.

“Cases are rising, and we expect to see a steady increase in transmission as BA.2 continues to circulate around the city,” he said. “We’ve all been through so much the last couple years, and we need every tool available to us. It’s crucial we all take the steps we know work to keep us safe and healthy, like getting vaccinated, boosted, tested, and wearing masks in settings where the vaccination status of those around you are unknown.”

For this reason, the mayor and Vasan are recommending New Yorkers wear masks when inside public spaces. However, the mayor didn’t make this an official mandate, simply a recommendation.

‘HOLD OFF’ ON LIFTING MASK MANDATE FOR YOUNGEST NEW YORKERS

While the mask recommendation is for New Yorkers of all ages, Adams said he wants to “hold off” on lifting the mask mandate for the city’s youngest students -- 2 to 4 years olds, which was slated to occur on Monday.

“We need to prepare, not panic. ...There are many risks we have to overcome with COVID, but we remain committed to assistance and responding as needed in New York City,” Adams said.

“We’re not going to sit around and wait; we’re going to be aggressive in our response. And as I say over and over again, ‘GSD,’ get stuff done.,” said Adams.

“...We’re going to be distributing 6.3 million free at home tests. ...We have an amazing team of men and women who are working around the clock to get this done. They [the at-home tests] will be provided to over 2,500 community organizations, libraries, cultural institution and houses of worship,” he added.

CASES RISING ACROSS THE CITY

This has led city officials to defer to the color-coded “COVID-19 Community Levels” system from the Centers for Disease Control and Prevention (CDC).

“We’re seeing cases rise across the city,” said Vasan. “You may recall we published a COVID color coded risk alert system a couple of weeks ago, which really looks at a combination of factors -- case thresholds, case transmission being one; hospitalization rate being another; bed occupancy space in our healthcare system being a third data point. We’re seeing cases rise across the city, and if they continue on this trajectory, we expect to move into a higher risk category in a matter of weeks.”

CALLING ON CONGRESS

Adams and city health leaders also called on all members of Congress to appropriate more than $15 billion in emergency funding for COVID-19. While New York City will continue providing testing and vaccine services to New Yorkers at no cost through NYC Health + Hospitals, “gridlock in Washington, DC has threatened the health of communities across New York and the rest of the nation,” Adams said.

Earlier this week, Adams met with the New York City congressional delegation and urged them to push for immediate passage of the COVID-19 aid package. As the city and the nation wait for action from certain members of Congress, Adams said New York is taking action to bolster preparedness efforts by distributing the at-home tests.

Adams said the more than $15 billion in funding Congress has yet to authorize has the potential to:

  • Impact the federal supply of vaccines and treatments;
  • Eliminate federal reimbursement to private providers for vaccination, testing, and outpatient treatment provided to uninsured people;
  • Reduce immediate access to services for testing, treatment, and vaccination, which could lead to delays in testing and care; and
  • Put the country at risk of losing its ability to develop and distribute vaccines for new variants in the future.