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Wednesday, May 19, 2021

Acceleron has positive prelim data in Phase 2 hypertension trial

 Treatment with sotatercept in the ongoing SPECTRA Phase 2 trial was associated with improvements in resting and exercise hemodynamics at week 24 –

– Sotatercept was generally well tolerated, consistent with the previously reported safety profile in PAH and in other diseases –

- Company-hosted investor and analyst conference call and webcast with guest PAH key opinion leader to be held today, Wednesday, May 19th at 10:30 a.m. EDT –

Detailed presentation is available on the "Publications" page under the "Science & Pipeline" section of Acceleron’s website, www.acceleronpharma.com.

https://finance.yahoo.com/news/acceleron-presents-preliminary-data-spectra-120000149.html

Thermo Fisher, UCSF to Open Cell Therapy Centerf

  Thermo Fisher Scientific Inc. (NYSE:TMO), the world leader in serving science, and the University of California, San Francisco (UCSF) today announced they have formed a strategic alliance to accelerate the development and manufacturing of cell-based therapies.

Under the agreement, Thermo Fisher will build and operate a 44,000-square-foot, state-of-the-art cell therapy development, manufacturing and collaboration center in leased space on UCSF's Mission Bay campus, which includes biomedical research facilities and hospitals. The site will offer clinical and commercial cGMP cell therapy manufacturing services, along with associated technology development support, to UCSF and other partners.

Expected to open in 2022, the facility will also serve as a central location where customers and UCSF researchers will have access to Thermo Fisher's broad portfolio of Cell Therapy Systems (CTS) reagents, consumables, and fit-for-purpose instrumentation and compliant software. The CTS product portfolio is designed to work together, and seamlessly transition from research to clinical manufacturing to address cell therapy production workflow challenges.

https://finance.yahoo.com/news/thermo-fisher-scientific-university-california-130000620.html

Anthem started at Overweight by Wells Fargo

 Target $460

https://finviz.com/quote.ashx?t=ANTM&ty=c&ta=1&p=d

Unitedhealth started at Overweight by Wells Fargo

 Target $478

https://finviz.com/quote.ashx?t=unh

Study shows AstraZeneca vaccine works well as third booster

 The COVID-19 vaccine of AstraZeneca Plc and Oxford University works well as a third booster dose, stepping up antibodies to the coronavirus spike protein among participants in a study, the Financial Times said https://www.ft.com/content/c5297d58-ad6d-490f-89e0-74f9c13377e4 on Wednesday.

The news comes as vaccine makers warn that the world will need yearly booster shots, or new vaccines, to tackle virus variants, although some scientists question if such shots are necessary.

The newspaper quoted a person familiar with the results of the study as saying it showed the antibody reaction to the booster shot was "strong enough against any variant" and put to rest fears that adenoviruses could not be used more than once.

AstraZeneca and Oxford University did not immediately respond to a Reuters request for comment on Oxford's yet to be published study.

The vaccine makes use of a new technology employing a modified version of adenoviruses, which cause the common cold, as vectors to ferry instructions to human cells.

This design led to concern among scientists that the doses could lose potency if annual inoculations become necessary to fight new variants.

It is not known when Oxford and AstraZeneca plan to publish study data, the paper added.

The European Union signed a new contract this month for 1.8 billion doses of the Pfizer-BioNTech vaccine to cover booster doses.

https://www.yahoo.com/news/study-shows-astrazeneca-vaccine-works-045909548.html

Bristol Myers expands deal with Exscientia, taking its AI R&D engine to next step

 One day after taking a shot on an anti-TIGIT bispecific from Agenus, Bristol Myers Squibb is still in a dealmaking mood.


For Wednesday’s chaser, Bristol Myers is returning to a company that had teamed up with Celgene before its acquisition in 2019. That biotech is Exscientia, and they’ve scored an expanded deal with Bristol Myers to further build on its artificial intelligence capabilities less than a month after a massive Series D financing.


The updated collaboration calls for “up to” a $50 million upfront payment to the Oxford, UK-based biotech, along with $125 million in “near to mid-term” milestones, the companies said in a release. Other milestones for regulatory and commercial aspects can bring the total value of the deal past $1.2 billion.



Exscientia didn’t immediately specify how many targets or indications will be involved in the partnership, saying only it will be “multi-target” and include “multiple therapeutic areas” such as oncology and immunology. Endpoints News has reached out for comment.


Over the last few years, AI deals have begun grabbing a bigger foothold throughout the biopharma industry. Several biotechs have also popped up promising to speed up the drug development process through machine learning and other AI-focused models, including players like insilico, Denovio and Genesis.


Bristol Myers has made these types of AI plays before, signing on to work with Concerto HealthAI in March 2019 to do just that. They also partnered with machine-learning startup Insitro in October 2020 to potentially find new ways to create drugs for ALS.


And AstraZeneca announced in February it added the first target generated by AI to its portfolio, coming out of a collaboration with the London-based company, BenevolentAI. That deal focused on identifying and validating a new way to attack chronic kidney disease.


Exscientia is no stranger to wheeling and dealing, having scored several major collaborations before its first major financing round about a year ago. The biotech netted partnerships with a host of Big Pharmas including Bayer, Roche, Sanofi and GlaxoSmithKline, not limiting their platform to one area: The deals ranged from cardiology and oncology to psychiatric and metabolic diseases.


Those deals also followed a team-up with Sumitomo Dainippon Pharma for an experimental pill in obsessive compulsive disorder, which the pair claim was the first AI-developed drug to enter the clinic when it began Phase I in early 2020.


But back in May 2020, Exscientia began hitting the gas in raising capital, netting a $60 million Series C to more than double their previous round from 2018. The Series C was ultimately expanded this past March when BlackRock pushed its total to $100 million, and Exscientia quickly raised another $525 million in late April — a raise that included a $252 Series D round, plus a $300 million equity investment by SoftBank.


The biotech has also continued to tout what it says are the first-ever experimental drugs to hit the clinic. In the vein of its OCD pill, Exscientia said in April that its AI-designed molecule for immuno-oncology is the first such compound to reach in-human testing in that area as well.

https://endpts.com/bristol-myers-expands-celgene-era-deal-with-exscientia-taking-its-ai-rd-engine-to-the-next-step/

BioXcel: FDA accepts application for med for schizophrenic, bipolar agitation

 FDA sets PDUFA action date for January 5, 2022

If approved, BXCL501 would represent the first major advancement in the acute treatment of agitation associated with schizophrenia and bipolar disorders in almost a decade

https://finance.yahoo.com/news/bioxcel-therapeutics-announces-fda-acceptance-110000657.html