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February 28, 2019

Today's Rundown

Featured Story

Bispecifics player Abpro teams up with China’s NJCTTQ in biobucks deal worth up to $4B

Abpro is partnering with China-based NJCTTQ to develop new bispecific antibodies using its antibody discovery platform. Under the agreement, Abpro could collect up to $4 billion, which includes $60 million in “near-term R&D funding,” as well as milestone payments and royalties.

Top Stories

Novavax plummets after another phase 3 RSV study miss, this time in infants

Once described as having the potential to become “the largest selling vaccine in the history of vaccines,” Novavax’s fusion protein nanoparticle shot against respiratory syncytial virus has missed another phase 3 trial, causing the company’s stock price to lose about two-thirds of its remaining value in premarket trading.

J&J bags option on AdoRx lung cancer drugs

Johnson & Johnson is teaming up with AdoRx Therapeutics to develop lung cancer drugs. The deal gives J&J an exclusive option to research, develop and commercialize AdoRx antagonists.

[Sponsored] Rise in Targeted Therapies Drives Need for Flexible, Small-Volume Manufacturing

Biologics have experienced steady double-digit growth over the last 15 years and now comprise slightly more than a quarter of all New Molecular Entity (NME) FDA approvals.

Horizon Pharma's inflammatory eye drug aces phase 3, poised for midyear BLA

Horizon Pharma’s inflammatory eye drug teprotumumab met its primary endpoint in a phase 3 study, with topline data showing the drug beat out placebo in reducing proptosis, or bulging of the eye. The candidate also met its secondary endpoints, and Horizon plans to submit a BLA in mid-2019.

Denali expands antibody discovery deal with AbCellera

Denali Therapeutics has expanded its antibody discovery deal with AbCellera. The agreement tasks AbCellera with generating panels of antibodies for up to eight targets picked by Denali.

Maze Therapeutics debuts with $191M to go after genetic modifiers

Maze Therapeutics aims to make sense of the proliferation of human genetic data that has emerged in recent years and understand how some genes provide protection against disease so that they can be targeted with drugs.

Axial Biotherapeutics nets $25M for clinical gut-brain axis studies into autism and Parkinson’s

Axial Biotherapeutics has raised $25 million to fund its programs aimed at the gut microbiome, for the treatment of Parkinson’s disease and autism spectrum disorder.

StemoniX rakes in $14.4M for micro-organ drug testing chips built from stem cells

Microtissue developer StemoniX has secured $14.4 million in funding to commercialize its organ-on-a-chip platforms for drug development.

Cohen drops testimony on Novartis deal: They wanted ‘access’ to Trump

In congressional testimony, Michael Cohen sketched out a relationship that contradicts Novartis' original version in some important ways—namely, regarding how often the company interacted with Cohen and what, exactly, Novartis wanted him to do.

Resources

[Research] Maximize Pharma Marketing ROI with Digital HCP Engagement

Which HCP Touchpoints and channels are yielding the best results in today’s digital world?

[Whitepaper] Cell-Based Cancer Immunotherapies: Commercial Risk, Curative Reward

White paper outlining the key types of cell-based immunotherapies in oncology, as well as the development and commercial outlook for each.

[Whitepaper] Better Market Intelligence With Smart Search

It’s never been more challenging to stay on top of trends and innovation shaping the future of healthcare. Discover how AI can help competitive intelligence teams achieve more proactive strategies.

[Whitepaper] Managing Demand Uncertainty in Biologics Production

When a biologics company prepares to launch a new product, it must forecast the manufacturing capacity it will need, factoring in its estimate of the size of future sales, the timing of the launch, the dosage of the product, its strategy for building its market and a host of other variables.

[Whitepaper] RTSM/IRT: A Roadmap For Developing Systems That Address Current Frustrations

92% of survey respondents make changes to their RTSM/IRT systems due to study changes. See what else puts a strain on their clinical trials. Download the Research Whitepaper.

[Whitepaper] Six API Challenges That could be Slowing your Development

Download this whitepaper to learn more.

[Whitepaper] Engaging Organized Customers in the Era of the Quadruple Aim

Explore how the pharma industry can adapt its approach to the changing healthcare marketplace in the era of the Quadruple Aim

[Whitepaper] Clinical Validation of a Powerful Immune Assay for Patient Selection

Learn how Health Expression Models provide increased sensitivity, specificity, and accuracy for characterizing immune response in solid tumor specimens.

[Whitepaper] Host Cell Protein Analysis in Biologic Drug Development

This whitepaper reviews fundamental aspects of HCPs that pertain to biologic drug development and presents current and emerging approaches to HCP analysis.

[Whitepaper] Integrating clinical research at the Point of Care—A New Operating Model

Clinical trials take too long and cost too much—here's what needs to change.

[Whitepaper] Accelerate Time To Market Working With Industry Specialist MSP

With FDA approval imminent, start-up Life Sciences company partners with an industry focused MSP to design and manage its regulated cloud-based infrastructure to speed time to market.

[Survey] Veeva 2019 Unified Clinical Operations Survey

Share your thoughts on the life sciences industry's progress in improving study execution.

[eBook] 2018 Weekly Compendium

The Biopharma industry is moving at lightning speed and it can be a challenge to keep pace. Here at Biotech Primer we spend hours each week researching, writing, and editing original content for the Biotech Primer WEEKLY with one goal in mind: to help everyone better understand the latest science and technology driving today’s healthcare industry.

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