Search This Blog

Wednesday, June 2, 2021

AstraZeneca in talks to shift COVID-19 vaccine production to Catalent factory

 AstraZeneca Plc is in talks with the U.S. government to shift production of its COVID-19 vaccine from a troubled Baltimore plant to a factory owned by Catalent Inc, the New York Times reported, citing people familiar with the matter.

The British drugmaker has been on the lookout for an alternative production site since the U.S. government stopped it from using Emergent BioSolutions Inc's Baltimore plant after workers accidentally contaminated a batch of Johnson & Johnson's vaccine with ingredients from AstraZeneca's that was also being produced at the time.

AstraZeneca's vaccine, approved in dozens of countries except United States, has been under increased scrutiny over reports of extremely rare but serious blood clots in the brain in some people who received the vaccine.

New Jersey-based Catalent will make use of its factory in Maryland where it already produces drug substance used in AstraZeneca's vaccine, the NYT report said on Wednesday.

AstraZeneca did not immediately respond to Reuters request for comment, and Catalent declined to comment.

https://www.marketscreener.com/quote/stock/ASTRAZENECA-PLC-4000930/news/AstraZeneca-nbsp-in-talks-to-shift-COVID-19-vaccine-production-to-Catalent-factory-NYT-35503394/

Morphosys mortgages its future

 It is worrying when a company once known for in-house development apparently has to resort to buying in late-stage development candidates – and perhaps more so when it raises the cash to do so by pawning the family silver. 

Certainly this is how Morphosys shareholders have reacted to the group's $1.7bn buyout of Constellation Pharmaceuticals, funded via a royalty-sharing deal with Royalty Pharma; Morphosys shares fell 16% at the open. But an analysis of Evaluate Pharma data suggests that this deal might not be all that unwise.

The purchase

Morphosys is paying $34 per share in cash for Constellation, a cancer-focused group whose lead candidate is pelabresib (CPI-0610), a BET inhibitor in a phase 3 trial in myelofibrosis. Constellation also has CPI-0209, an EZH2 inhibitor, in phase 2 in solid tumours and lymphoma, plus a couple of preclinical programmes. 

Though the price per share came in at a 68% premium to Constellation’s close yesterday it is worth noting that Morphosys waited until its target was off the boil. In mid-February Constellation’s stock was trading at nearly $37. 

Upon the Constellation acquisition closing, Morphosys’s other deal kicks in. Royalty Pharma will hand over $1.4bn up front and give Morphosys access to up to $350m in development funding bonds, which can be drawn over the course of a year, plus potential milestones. 

The price

In return, Royalty Pharma gets a generous share of Morphosys’s income: all of its royalties on Tremfya, the psoriasis blockbuster licensed to Johnson & Johnson, for a start. It will also receive shares of any future royalties on three of Morphosys’s clinical projects as well as two of Constellation’s.

But a look at the net present value of these assets, as calculated by Evaluate Omnium, suggests that Royalty has either paid over the odds or has major faith in what these projects can achieve. 

Crunching the numbers on Morphosys's Constellation deal
ProjectPhase and indicationNPV attributable to Morphosys% to go to Royalty PharmaTotal
TremfyaMarketed, plaque psoriasis and psoriatic arthritis $731m100% royalties$731m
OtilimabPh3 in rheumatoid arthritis; Ph2 in Covid-19 $82m90%*$74m
GantenerumabPh3, Alzheimer's$4m60% royalties$2m
Pelabresib/CPI-0610 (Constellation)Ph3, myelofibrosis$1,548m3% of sales$46m
CPI-0209 (Constellation)Ph1/2, solid tumours and diffuse large B-cell lymphomaN/A3% of sales$0m
NPV attributable to Royalty Pharma$854m
Total paid by Royalty Pharma$1,425m
*80% royalties & 100% of milestones to go to Royalty. Source: Evaluate Omnium, clinicaltrials.gov & company release.

If the sellside’s forecasts for these compounds are accurate Royalty’s up-front fee alone is worth $571m more than its share of their royalties is likely to bring in. 

Does Royalty know something equity analysts do not? It must reckon that the assets still in R&D can succeed beyond what the sellside models – a brave bet indeed considering that one of them, gantenerumab, is in development for Alzheimer’s. 

https://www.evaluate.com/vantage/articles/news/deals/morphosys-mortgages-its-future

FDA approval tracker: May

 Last month ended with a flurry of US FDA decisions and one, the green light for Amgen’s Lumakras, came over two months early. The accelerated approval in NSCLC patients with a Kras G12C mutation was given to the 960mg dose; a 240mg dose is the subject of a postmarketing study to see whether it has a similar clinical effect. Two other oncology drugs gained first-time accelerated approvals: J&J’s Rybrevant and Bridgebio’s Truseltiq. Both have confirmatory trials under way. After two previous complete response letters it was finally good news for Heron’s pain therapy Zynrelef, an extended-release bupivacaine combined with the anti-inflammatory meloxicam. To try and gain market share Heron is pricing Zynrelef at a 22-28% discount to Pacira’s Exparel; Evercore ISI analysts note that this price will also allow Heron’s drug to compete with generic bupivacaine. With May now over all eyes rest on aducanumab’s June 7 Pdufa, the biggest regulatory event of the year (Go or no go? Aducanumab’s day of reckoning, May 27, 2021).

Notable first-time US approval decisions in May
ProjectCompanyIndication2026e sales by indication ($m)Outcome
Lumakras
(sotorasib)
AmgenNSCLC with Kras G12C mutation after at least one systemic therapy1,756Approved (~2.5mth early, accelerated)
Myfembree (relugolix)MyovantUterine fibroids490Approved
Zynrelef
(HTX-011)
Heron TherapeuticsPost-op pain relief471Approved
Lybalvi
(ALKS 3831)
AlkermesSchizophrenia and bipolar 1 disorder380Approved
Empaveli (pegcetacoplan)ApellisPNH (including treatment naive)309Approved
Truseltiq
(infigratinib)
Bridgebio Pharma2L cholangiocarcinoma253Approved (accelerated)
Rybrevant
(amivantamab)
J&JNSCLC with EGFR exon 20 insertion mutations250Approved (~2mth early, accelerated)
Pylarify (PyL)Lantheus HoldingsProstate cancer diagnostic imaging agent233Approved
Zonisamide oral suspensionEton/Azurity PharmaceuticalsPartial seizures in epilepsy-No decision yet
Dehydrated alcohol injection (DS-100)EtonMethanol poisoning-CRL (CMC)
CamceviForesee PharmaceuticalsAdvanced prostate cancer-Approved
Source: Evaluate Pharma & company releases.

 

Advisory committee meetings in May
ProjectCompany2026e sales by indication ($m)OutcomeNote
Vynpenta
(avacopan)
Chemocentryx639Efficacy vote split (9-9), safety profile and benefit-risk votes slightly in favour (10-8)ANCA-associated vasculitis, Pdufa in July (Chemocentryx’s future in doubt as avacopan foundation crumbles)
Teplizumab
(PRV-031)
Provention Bio-Voted 10-7 that benefits outweigh risks in support of approval Delay of clinical type 1 diabetes in at-risk individuals (Provention’s diabetes project takes a tentative step forward)
Source: Evaluate Pharma & FDA adcom calendar

 

Supplementary and other notable approval decisions in May
ProductCompanyIndication (clinical trial)Outcome
OpdivoBristol Myers SquibbAdjuvant oesophageal/gastroesophageal junction cancer (Checkmate-577)Approved
ZeposiaBristol Myers SquibbUlcerative colitis (True North)Approved
Nurtec ODTBiohavenPrevention of migraine (Study 305201)Approved
FerriproxChiesiTransfusional iron overload due to sickle cell disease or other anaemias in adults and paediatrics aged 3 and olderApproved
Keytruda + Herceptin + chemoMerck & Co1L Her2+ gastric or gastroesophageal junction adenocarcinoma (Keynote-811)Approved (accelerated)
CosentyxNovartisModerate-severe plaque psoriasis in children and adolescents (NCT03668613NCT02471144)Approved
NuzyraParatekOral only dosing regimen for the treatment of community-acquired bacterial pneumoniaApproved
MSB11455 (Neulasta biosimilar)FreseniusReduce the incidence of infection associated with febrile neutropeniaNo decision yet
EsbrietRocheUnclassifiable interstitial lung disease (NCT03099187)No decision yet
AubagioSanofiPaediatric relapsing MS (Terikids)No decision yet
AlecensaRocheFirst-line Alk-positive NSCLC (Bfast)No decision yet
Source: Evaluate Pharma & company releases.

 

FDA Covid-19 EUAs
ProductCompany2026e sales by indication ($m)Note
ComirnatyPfizer1,784Expanded to include 12 to 15-year-olds
Sotrovimab
(VIR-7831)
Vir/GSK1,212Treatment of mild-moderate Covid-19 in adults and paediatrics (US appetite for Covid-19 treatments remains undiminished)
Source: Evaluate Pharma & company releases.

https://www.evaluate.com/vantage/articles/news/snippets/us-fda-approval-tracker-may-0

Biggest Challenge Biogen Will Face if Its Alzheimer's Drug Is Approved

 A crucial decision is days -- or maybe even hours -- away for Biogen (NASDAQ:BIIB). By June 7, the Food and Drug Administration will decide whether to approve the biotech company's controversial Alzheimer's drug candidate. A positive decision seems crucial for Biogen because the company predicts declining sales of its big multiple sclerosis blockbuster and is in need of a new growth driver.

If the FDA gives the nod to the Alzheimer's candidate, aducanumab, it's very likely Biogen shares will soar. More than 6 million Americans suffer from the disease, and treatment options are extremely limited. But Biogen might not get the major revenue boost it's hoping for even if aducanumab wins approval. Let's look at the biggest challenge the company could face.


Patient groups and families eagerly await the aducanumab regulatory decision. If approved, it would be the only treatment known to reduce declines in daily function and cognition. But Biogen's challenge may be convincing doctors to prescribe aducanumab to their patients.

Why would doctors refuse to prescribe such a treatment? Many are hesitant due to the drug candidate's clinical trial path. I'll explain:

Biogen halted clinical trials of aducanumab in early 2019. This came after a futility study saying the treatment was unlikely to work. The company surprised investors later in the year when it revived the program -- and said it soon would file for regulatory approval.

The reason for such a turnaround? Biogen conducted a post-study analysis of its two phase 3 trials. Initially, the trial named Emerge met its primary endpoint. It showed a reduction in clinical decline. Researchers measure that by looking at cognition and daily function. The trial named Engage didn't meet this endpoint. But in the post-study analysis, Biogen looked at a group of some Engage participants who received higher doses of the drug candidate. And those participants showed a reduction in clinical decline, the company said.

Are the data enough?

Since Biogen reinstated the aducanumab program, analysts and doctors have argued about whether data from a post-study analysis are strong enough to support regulatory approval. In fact, an FDA advisory committee that was convened late last year even voted against approving the drug candidate. The FDA considers the opinion of this panel of experts but isn't obliged to follow it.

If we look at market potential without the idea of whether doctors will or won't prescribe the drug, it's big. Aducanumab could generate about $4.9 billion in annual sales by 2026, according to the news site EvaluatePharma. And some news reports cite analyst estimates of at least $10 billion in annual sales.

Now, let's get back to the subject of what doctors will decide to do. Right now, it's fair to say that aducanumab is controversial and some healthcare professionals aren't convinced of its efficacy; the FDA advisory committee vote is an example of that. A report co-authored by Dr. David S. Knopman, a site investigator in the aducanumab trials, calls for another phase 3 trial of aducanumab to support the idea of a higher dose.

So, what does this mean for Biogen?

If the FDA approves aducanumab, Biogen investors surely will cheer. It does offer the company another revenue opportunity. But I would have preferred that Biogen took its time with this one and conducted another phase 3 trial, as Dr. Knopman and his fellow authors recommend. Right now, if aducanumab is approved, Biogen may face an uphill battle winning over the majority of doctors. Another phase 3 trial with strong results would have made it much easier to convince doctors of the drug's merit.

This doesn't mean a potential aducanumab approval would be bad news. But it does mean the drug's success isn't guaranteed. And if success does happen, it will take time. Meanwhile, if revenue disappoints in the first couple of quarters, shares of this biotech giant might suffer.

So if you're a Biogen shareholder (or want to become one), it's important to keep an eye on these first quarters. They would offer us clues about whether doctors are willing to give the product a chance -- and whether Biogen may indeed have a major new revenue driver.

https://www.fool.com/investing/2021/06/02/heres-the-biggest-challenge-biogen-will-face-if-it/

MorphoSys to Acquire Constellation Pharma

 Accelerates Growth Strategy by Adding Two Mid- to Late-Stage Product Candidates: Pelabresib (CPI-0610) and CPI-0209

Bolsters Position in Hematology-Oncology and Expands into Solid Tumors

Best-in-Class Combined Discovery and Development Capabilities Accelerates Ability to Provide New Cancer Treatments to Patients

MorphoSys Enters into Strategic Funding Partnership with Royalty Pharma

MorphoSys to Host Conference Call and Webcast at 2:00 PM CEST / 8:00 AM EST Today

MorphoSys AG (FSE: MOR; NASDAQ: MOR) ("MorphoSys"), and Constellation Pharmaceuticals, Inc., (NASDAQ: CNST) ("Constellation") today announced that they have entered into a definitive agreement whereby MorphoSys will acquire Constellation for $34.00 per share in cash, which represents a total equity value of $1.7 billion. The transaction has been unanimously approved by the management board (Vorstand) and the supervisory board (Aufsichtsrat) of MorphoSys, as well as the Board of Directors of Constellation and is expected to close in the third quarter of 2021.

Constellation is a clinical-stage biopharmaceutical company using its expertise in epigenetics to discover and develop novel therapeutics that address serious unmet medical needs in patients with various forms of cancer. Constellation’s two lead product candidates, pelabresib (CPI-0610), a BET inhibitor, and

CPI-0209, a second-generation EZH2 inhibitor, are in mid- to late-stage clinical trials and have broad therapeutic potential to offer meaningful benefits to patients with various hematological and solid tumors. Pelabresib has the potential to be a first- and best-in-class BET inhibitor and is currently in Phase 3 clinical trials for myelofibrosis, a bone marrow cancer that disrupts the body’s normal production of blood cells. CPI-0209 is currently in Phase 2 with best-in-class potential for treating hematological and solid tumors. Constellation’s pipeline also includes numerous preclinical compounds.

Conference Call

MorphoSys will host a conference call and webcast to discuss the transaction on June 2, 2021 at 2:00 p.m. CEST, or 8:00 a.m. EDT. The webcast and accompanying slides can be accessed in the Media and Investors section, under Conferences, of MorphoSys’ website at http://www.morphosys.com or at http://morphosys-constellation-royaltypharma.com/. After the call, a slide-synchronized audio replay of the conference will be available at the same location.

The live call is also available at:

Germany:

+49 69 201 744 220

For UK residents:

+44 203 009 2470

For US residents:

+1 877 423 0830

Participant PIN:

78217587#

Please dial in 10 minutes before the beginning of the conference.

https://finance.yahoo.com/news/morphosys-acquire-constellation-pharmaceuticals-112500240.html

Disney Cruise Line to set sail on 2-night COVID test cruise

 After a catastrophic coronavirus cruise season, Disney Cruise Line will finally set sail later this month, the company said in a statement Tuesday.

The Centers for Disease Control and Prevention approved the cruise line’s request to conduct a two night simulation cruise on June 29 on the Disney Dream departing from Port Canaveral.

The federal government is getting ready to let cruises sail again, but only if nearly all passengers and crew are vaccinated against the virus. Republican Gov. Ron DeSantis, however, signed a bill banning business from requiring proof of vaccination, so cruise lines must prove the effectiveness of their COVID-19 safety protocols on test cruises.

“We have reached an important next step toward our gradual and responsible resumption of service, and are grateful for the productive dialogue with state, local and federal officials,” Disney Cruise Line spokeswoman Cynthia Martinez said in an email.

Miami-based Norwegian has threatened to abandon its three Florida ports and move to the Caribbean over DeSantis’ order. But the governor was unyielding, saying there were plenty of other cruise lines eager to take its place.

Norwegian is the third-largest cruise line in the world and has ports in Miami, Port Canaveral and Tampa. It also makes stops in Key West.

DeSantis is suing the Centers for Disease Control and Prevention over the no-sail order. The CDC is set to let cruises sail again if 98% of the crew and 95% of passengers are vaccinated and ships take other measures to limit the risk of transmitting the virus.

https://apnews.com/article/fl-state-wire-business-lifestyle-travel-health-34e4ecfdb4d632984cc3b130eb31d076

Moderna Signs New Drug Substance Production Deal With Lonza In Netherlands

  Covid-19 vaccine maker Moderna Inc. (MRNA) announced Wednesday that it has entered into an additional agreement with Lonza Group AG (LZAGF.PK), a supplier to the pharmaceutical, healthcare and life-science industries, to support drug substance manufacturing for its global supply chain.

The agreement will establish a new production line at Lonza's Geleen site in the Netherlands, contributing to the supply of an additional 300 million doses of Moderna's updated booster variant vaccine candidate, if authorized, per year, at a 50 g dose.

With the latest deal, Moderna now expects to be able to supply the equivalent of 600 million 50 g doses per year from production within the European Union. The company earlier announced investments in drug substance manufacturing with ROVI in Granada, Spain.

Both these new drug substance lines in the European Union are expected to be operational before the end of 2021.

https://www.nasdaq.com/articles/moderna-signs-new-drug-substance-production-deal-with-lonza-in-netherlands-quick-facts