FDA’s Pazdur clamps down on accelerated approvals

Today's Big News

Nov 18, 2022

Elizabeth Holmes sentenced to 11+ years in prison for defrauding Theranos investors

With Sanofi as its marketing partner, Provention Bio grabs long-awaited FDA nod for diabetes drug 

FDA wants confirmatory trials to be underway before granting accelerated cancer nods, Pazdur says 

Repeat COVID-19 infection deadlier than the first go-round, says study 

Lysogene’s lead gene therapy flunks phase 2/3 trial almost a year after Sarepta walked out 

 

Featured

Elizabeth Holmes sentenced to 11+ years in prison defrauding Theranos investors

Elizabeth Holmes, founder of the once high-flying blood-testing startup Theranos, was sentenced to 11.25 years in prison Friday after being convicted of fraud.
 

Top Stories

With Sanofi as its marketing partner, Provention Bio grabs long-awaited FDA nod for diabetes drug

The FDA has approved Provention Bio’s Tzield to delay the progression of type 1 diabetes. It will be available to patients age 8 and older who are in stage 2 of the disorder. With the approval, Tzield becomes the first drug approved to delay the onset of type 1 diabetes.

FDA wants confirmatory trials to be underway before granting accelerated cancer nods, Pazdur says

The FDA's oncology department, under the leadership of Richard Pazdur, M.D., has started putting an emphasis on timely confirmatory trials as a condition for accelerated approvals. But that's not a one-size-fits-all piece of guidance, Pazdur said in an interview with Fierce Biotech.

Repeat COVID-19 infection deadlier than the first go-round, says study

Reinfection with SARS-CoV-2 significantly increases death and hospitalization rates, according to a recent study.

Lysogene's lead gene therapy flunks phase 2/3 trial almost a year after Sarepta walked out

Lysogene funds are dwindling as the company reported disappointing phase 2/3 data of its lead gene therapy. The therapy was found to be clinically significant in the youngest patients but not among the majority of trial participants.

Sema4 lays off another 448 employees amid exit from reproductive health testing

Sema4 will shut down its reproductive health testing and services division by early next year, eliminating about a third of its workforce in the process. The company joins a handful of other developers that have slimmed down rosters amid less-than-stellar third-quarter earnings reports.

Apellis' closely watched eye drug gets new FDA goal date after changes to its filing scared investors

After some investor clamor, Apellis Pharmaceuticals’ blockbuster hopeful eye drug pegcetacoplan is back on the FDA’s review track.

'I would put us up against mRNA': Novavax sets out vision for vaccine success in COVID and beyond

While it looks like Novavax has been late to the party when it comes to gaining COVID market share, the company's executives told Fierce Biotech that they’re playing the long game.

Primary care physician burnout raging across the US and other high-income countries, Commonwealth Fund finds

A new survey of more than 9,500 international primary care physicians highlights unmet mental health needs and a looming clinician shortage should the U.S. fail to take action.

FDA looks to bypass cancer drugs' companion diagnostics with new pilot program: Pazdur

Existing cancer companion diagnostics are bundled with the specific cancer drugs they’re approved for. But the FDA is looking to get around this one-drug-one-test situation by looking at “minimal performance criteria” of tests, FDA oncology chief Richard Pazdur, M.D., said.

Lilly wades deeper into copycat insulin market, scoring interchangeability tag for Lantus biosim

The FDA has blessed Eli Lilly’s approved insulin biosimilar Rezvoglar with an interchangeability tag, which means the product can be swapped out for its brand-name counterpart right at the pharmacy counter. The nod comes as insulin costs garner public, political and even pharma industry scrutiny.

HLTH22: Private equity rebuffs critics, says it brings rigor, scale and necessary change to healthcare

"Bad actors" are the minority, PE leaders said this week at HLTH 2022, touting a focus on responsible growth and increasing emphasis on ESG goals.

Inovio drops Lassa, MERS vaccines as clinical data fall short, gutting infectious disease pipeline

Inovio’s Lassa fever and Middle East respiratory syndrome vaccine candidates have fallen short of the bar set by the biotech’s partner, prompting the collaborators to pull the plug on the programs after getting a look at clinical data.
 
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'The Top Line': Celebrating the Fiercest Women in Life Sciences

This week on “The Top Line,” we share this week's headlines and discuss the 2022 honorees in our annual Fiercest Women in Life Sciences report.

 

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