Phenomic inks 2nd deal in 2 days

Today’s Big News

Nov 30, 2023

After watching Merck's chronic cough drama, GSK knew exactly what not to do with Bellus asset


AbbVie’s lung cancer data light path to ADC accelerated approval but fall short of earlier benchmark


Phenomic AI inks second deal in two days while Shape stretches Roche collab


Cybin turns in phase 2 depression data on psychedelic treatment, investors tune out


Sagimet's NASH drug-GLP-1 combo outperforms either alone for fibrosis


A protein inhibited by GSK's Rukobia could be culprit behind HIV comorbidities, study suggests


Merck turns to Acclinate to increase African American participation in cancer trials

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Featured

After watching Merck's chronic cough drama, GSK knew exactly what not to do with Bellus asset

By the time GSK sealed the deal on Bellus Health in April, the U.K. pharma knew exactly what not to do with the phase 3 chronic cough program. The company had watched Merck & Co. struggle with a rival med called gefapixant, taking notes.
 

Top Stories

AbbVie’s lung cancer data light path to ADC accelerated approval but fall short of earlier benchmark

AbbVie has its eyes on accelerated approval of its c-Met antibody-drug conjugate (ADC). The candidate achieved a 35% response rate in a subset of lung cancer patients, spurring plans to talk to regulators, but unfavorable comparisons to an earlier data drop partly took the shine off the update.

Phenomic AI inks second deal in two days, Shape stretches Roche collab

Phenomic AI went from radio silence to two deals in two days, this time signing an antibody-focused pact with Astellas. ShapeTX has also been busy, expanding an existing collaboration with Roche to tack on another target.

Ethical, Regulatory, and Operational Considerations for Cell and Gene Therapy Research in Children

Pediatric CGT trials have the potential to cure diseases and prolong lives. Discover steps to protect safety and enhance operations in your CGT trials.

Cybin turns in phase 2 depression data on psychedelic treatment, investors tune out

Cybin has put out more data on its psychedelic treatment for depression, presenting clinical data from a phase 2 trial that suggest there may be benefits to repeat administration but not to increasing the dose.

Sagimet's NASH drug-GLP-1 combo outperforms either alone for fibrosis

Just as things were getting overheated in the nonalcoholic steatohepatitis (NASH) drug space, GLP-1 receptor agonists showed up to the party with the potential to treat some symptoms of the chronic liver disease. Now, preclinical data from Sagimet Biosciences hints that when it comes to treating NASH, blockbuster GLP-1 drugs like Novo Nordisk’s semaglutide may be more of an ally than a threat to pharma companies pursuing the indication. 

A protein inhibited by GSK's Rukobia could be culprit behind HIV comorbidities, study suggests

New findings from researchers at the University of Montreal Hospital Research Centre suggest that a protein called gp120 might be a key culprit behind comorbidities associated with HIV.

Merck turns to Acclinate to increase African American participation in cancer trials

Against a backdrop of Big Pharma’s slow progress to increase the diversity of clinical trials, Merck & Co. has teamed up with digital health company Acclinate to try and enroll more African American patients in its cancer drug studies.

AbbVie pays $10B to acquire ImmunoGen, doubling down on red-hot ADC cancer field

The sizzling antibody-drug conjugate field is at the center of another major life sciences deal. Hoping to redeem itself following the epic Rova-T failure, AbbVie is shelling out $10.1 billion in cash to acquire ImmunoGen, maker of the ovarian cancer treatment Elahere.

Bayer taps CrossBay’s uterus access device to make IUD placements less painful

CrossBay’s approach does away with the metal forceps typically needed to reach the inner uterus and has collected clearances in endometrial biopsies and IVF procedures.

Experimental gene therapies on the cusp to ‘disrupt’ Gaucher disease drug market: GlobalData

As gene therapies ramp up in spinal muscular atrophy and hemophilia, it may soon be the turn of Gaucher disease patients to realize the latent potential of this type of treatment.

As FDA probes CAR-T safety, expert meeting for Bristol's Abecma could serve as key guidepost

As industry watchers deliberate the implications from the FDA's investigation into secondary cancer risks from CAR-T medicines, an upcoming expert meeting could offer precious clarity from drug regulators.

Mayo Clinic unveils $5B, 6-year renovation of its flagship Rochester campus

The nonprofit will add five new buildings spanning 2.4 million square feet, two of which will be clinical facilities with designs intended to support continuous, tech-enabled care.
 
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Alzheimer’s breakthroughs, Leqembi's potential and what's next

This episode of "The Top Line" is dedicated to Alzheimer’s disease, spotlighting the latest treatments and what lies ahead. Fierce Pharma's Fraiser Kansteiner discusses Leqembi's full approval with Eisai's Alexander Scott. Annalee Armstrong from Fierce Biotech interviews Alzheimer's expert Howard Fillit, M.D., exploring groundbreaking research. Fierce Pharma’s Eric Sagonowsky speaks with Reisa Sperling, M.D., about Leqembi's potential in preventing Alzheimer’s progression before symptoms emerge.

 

Resources

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Accelerate drug discovery with high-performance computing (HPC) powered by the cloud

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Effective Technology Transfers for Mammalian-Derived Biologics

As a leader of technology transfer activities in the industry, Lonza understands the challenges associated with this critical step. Download this White Paper today to learn more. 

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An Introduction to Organ-on-a-Chip Technology

Emulate in vivo biology with next-generation in vitro technology.
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Overcome Challenges and Secure Successful Technology Transfers of Complex Biological Products in Sterile Manufacturing

A critical area to consider in selecting a CDMO is their ability to successfully complete technology transfers, which involves an intricate set of activities and disciplines that, if done incorrectly, could result in delays and failures that impact the overall success of your end product. Recognizing what it takes to complete this process effectively and efficiently is crucial to selecting the best partner for your project and product needs. This white paper delivers an analysis of critical success factors for effective technology transfer.
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Enhance the cost-effectiveness of your GMP chemical supply chain

Learn how to develop a high-performing supply chain for cGMP chemicals used throughout your bioprocessing workflows.
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Plasmid DNA Design Considerations for Cell and Gene Therapy

Download our whitepaper to learn about plasmid DNA design considerations for cell and gene therapy applications.
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Artificial Intelligence in Healthcare & Medical Affairs

This paper explores AI’s potential impact on healthcare and on Medical Affairs (MA) more specifically. It also outlines what MA teams can do now to proactively leverage AI to improve service to their stakeholders.
 

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