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January 03, 2020

With 45 new drugs receiving the FDA’s green light in 2019, it looks like the agency’s rate of approvals has bounced back. Though not a record, last year continues a trend up from 2016’s 22 new therapies. Novartis emerged as a big winner, with six approvals across multiple disease areas, including its gene therapy Zolgensma. And with the agency’s OK coming faster and more frequently, some are wondering if this is a sign of a “friendlier” FDA. Our special report is below.

Featured Story

Special Report—With 45 new drug approvals in 2019, ‘friendly’ FDA is here to stay

It looks like drug approvals have well and truly bounced back. 2019’s total of 45 approvals may not have hit the record high posted in 2018, but it fits into a general upward trend. Some pin that on a “friendlier” FDA, while others think it is the natural outcome of the maturation of new treatment approaches.

Top Stories Of The Week

After Audentes buy, acquisitive Astellas snaps up CAR-T biotech

Parker Institute-backed biotech Xyphos has been bought out by Japanese pharma Astellas as it looks to bolster its cancer pipeline.

First generics to Bristol-Myers and Pfizer's Eliquis are here. But can they launch before 2026?

The FDA touted approvals for the first two copycats to blockbuster blood thinner Eliquis, a major growth driver for Bristol-Myers Squibb and partner Pfizer as well as the overall biopharma sector. But ongoing patent lawsuits might prevent their launch until 2026.

Rise, Sir Pangalos! AstraZeneca R&D lead knighted

One of AstraZeneca’s top research leaders has been knighted in the U.K.’s New Year 2020 Honours list.

No holiday gift for GSK: FDA sends long-acting HIV injectable back to work

HIV patients looking for relief from the burden of daily pills will have to wait a little longer. Saturday, GlaxoSmithKline’s ViiV Healthcare said that the FDA had rejected its long-acting HIV injection, known under the working title Cabenuva. The statement is thin on details, only that the complete response letter is related to chemistry manufacturing and controls.

As promised, Gilead and Galapagos file filgotinib to FDA and get a speedy review

Gilead emerged from a meeting with the FDA this summer confident it would file for approval in the U.S. by the end of 2019: With just over a week to spare, it’s delivered on that promise.

AstraZeneca, Daiichi notch blockbuster FDA nod for breast cancer med Enhertu

For metastatic breast cancer patients who try and fail on multiple treatments, finding options to manage disease is a difficult proposition. AstraZeneca and Daiichi Sankyo hoped their antibody-drug conjugate could help that tough-to-treat population––and the FDA agreed to give it a shot despite a shaky safety profile. 

Blood testing nears a turning point as the evidence becomes undeniable

Blood testing is ubiquitous, but it’s clear its possibilities are unfulfilled. The field has seen setbacks, with Theranos’ well-known rise and fall, but a steady march of clinical data, engineering successes and FDA backing have shown that these ideas can work when they're done right.

Allergan scores year-end FDA nod for CGRP migraine med Ubrelvy, plans early 2020 launch

The CGRP migraine prevention field already has three meds from Amgen, Eli Lilly and Teva vying for market share, and now Allergan has scored the first approval for an oral CGRP to treat migraines as they happen. The med is expected to face 2020 competition from Biohaven’s rimegepant.   

Immuno-oncology combo targeting rogue enzyme in glioblastoma extends survival in mice

Researchers at MD Anderson Cancer Center discovered that a macrophage expressing the immune-suppressing enzyme CD73 is abundant in glioblastoma tumors and may be responsible for resistance to drugs that inhibit the checkpoints PD-1 and CTLA-4. Blocking CD73 in mouse models of the disease improved survival among animals given checkpoint inhibitors.

UCB to build €300M biologics plant, add 150 workers

UCB, which recently pulled off a $2.5 billion deal for an autoimmune drug candidate, says it sees the need for more biopharma production. To fill it, it will build a €300 million ($333 million) facility and staff it with 150 new workers.

Your FiercePharma reading list for long winter nights, no candle required

Light in the darkness. It’s a common theme this time of year. At their best, biotech and pharma are like the candles in Vermont windows, visible from a half-mile away. For patients with rare, deadly and chronic diseases, new treatments offer the hope of relief, or even a cure.

FierceBiotech's top 10 stories of 2019—Gilead's failure, Biogen's phoenix, JPM venue fatigue and more

As we reach the end of the year, we look back on the most read stories of the last 12 months as we also look ahead not just to a new year, but a new decade. So, what were the most read stories that you, dear reader, sought to end the 2010s with?

FierceMedTech's top 10 of 2019—Looking toward a new decade on the cutting edge

As we close out this decade, our biggest medtech stories of the past year have all looked toward what’s coming next—whether it’s new treatments or renewed companies, the common thread running through our most popular reads is that people are eager to see these advancements realize their promise.

Enrollment Showcase

Online Graduate Programs Designed for Your Career

Drexel University’s online graduate programs in biomedicine, clinical research, drug discovery, and molecular medicine were developed with working professionals in mind, providing you with the education, practical skills, and competitive edge you need to be successful in your career.  Learn more.

Resources

[Whitepaper] Digital Disruption in Biopharma: How Digital Transformation can reverse declining ROI on R&D

The beginning of this digital transformation is well underway and is likely to accelerate. Read our white paper, “Digital Disruption in Biopharma: How Digital Transformation can reverse declining ROI on R&D,” to learn more.

[Whitepaper] Are We Transforming in the Right Way? Why Launches Can’t Be Distracted By Empty Promises.

How are your launch strategies can convert “innovation” into value for patients?

[Whitepaper] How to Protect your Supply Chain from Security and Compliance Threats Utilizing On-Dose Authentication Technologies

Learn more: Best practices for defending supply chain security and compliance by efficiently managing product authentication.

[Whitepaper] The Unexpected Key to Building Value in Drug Discovery and Development

Small or emerging pharmaceutical and biotech companies pursuing novel molecules and targets have two important goals: achieve clinical success and attract new rounds of funding. While there’s never a guarantee of either, certain actions can influence the outcome in your favor.

[Executive Summary] Clinical Supplies - Made to Order

Learn how recent innovations in demand-led supply and direct-to-patient distribution are converging to create a next-generation clinical supply chain that is flexible, lean and most importantly patient-centric.

[Whitepaper] Digital Twins: Creating Digital Operations Today to Deliver Business Value Tomorrow

This whitepaper highlights the challenges of implementing the right digital twin strategy while providing key use cases in the manufacturing domain for which a digital twin is extremely useful and several examples of technology trends that will shape the future.

[Whitepaper] Q2 2019 Life Sciences M&A notes and trends

Get your copy of the Q2 2019 Life Sciences M&A notes and trends to understand the mergers and acquisitions (M&A) activity in the life sciences sector which drove 136 new M&A deals and provides a forward look to 2020 activity ahead.

[Whitepaper] What You Need to Know to Avoid Costly Delays in Your API Scale-Up

Are you facing costly delays in your API scale-up?

[Q&A] Embarking Upon the Commercial Manufacturing Journey for a Biologic

In this Q&A, four Catalent Biologics experts share how scale-up, regulatory expectations, demand forecasting and process validation all play a role in the success of a biologic when embarking upon the commercial manufacturing journey.

[Whitepaper] Modernizing clinical trials with Amazon Web Services (AWS)

From IoT to data management to high-performance computing and machine learning, leading life sciences organizations are using Amazon Web Services (AWS) to develop scalable, global, predictable, and secure solutions to modernize clinical trials while mitigating risks

[Whitepaper] The Impact of Step-Therapy Policies on Patients

Download this complimentary paper that explores the practice of step therapy and its impact on key stakeholders in the US healthcare system.