No new trials will be launched at this time: NIH

Today’s Big News

Jan 28, 2025

BioAge axes obesity asset over liver toxicity, pivots to preclinical prospects


Atalanta loads crossbow with $97M, targeting neuro trial starts for 2 RNAi therapies


Versant launches another obesity biotech with $65M series A and 'clinic-ready' GIP antibody


'No new studies are being launched': NIH explains the impact of Trump administration’s freeze


Leap crashes as midphase data mark end of gastric cancer program


Tris builds clinical case for opioid alternative by showing its pain drug is less likely to be abused


UPDATED: Cell therapy biotech Aurion eyes IPO despite legal pushback from investor


Longtime manufacturer ITM's lead radiotherapy outperforms standard of care in phase 3 neuroendocrine tumor trial


Takeda regains home rights to phase 3-stage depression drug from Neurocrine

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BioAge axes obesity asset over liver toxicity, pivots to preclinical prospects

BioAge Labs has given up on its lead obesity candidate. Weeks after stopping a trial in response to phase 2 data, the biotech has jettisoned the molecule and shifted its focus to a preclinical neuroinflammation prospect.
 

Top Stories

Atalanta loads crossbow with $97M, targeting neuro trial starts for 2 RNAi therapies

Atalanta Therapeutics has bagged $97 million, money the biotech plans to use to launch clinical trials for its small interfering RNA (siRNA) candidates in epilepsy and Huntington’s disease.

Versant launches another obesity biotech with $65M series A and 'clinic-ready' GIP antibody

Two months after launching Pep2Tango, VC firm Versant Ventures is unveiling another obesity-focused biotech in the form of Helicore Biopharma.

Transforming life sciences with AI, powered by Salesforce Life Sciences Cloud

Drug development and commercialization leads to tremendous advances in medicine and improvements to everyday life, but it often comes at a cost.

'No new studies are being launched': NIH explains the impact of Trump administration’s freeze

Just days after President Trump imposed broad restrictions on communications, meetings, travel and public appearances at the Department of Health and Human Services (HHS), the National Institutes of Health (NIH) is clarifying the extent of the freeze’s effect.

Leap crashes as midphase data mark end of gastric cancer program

Leap Therapeutics has come crashing down to earth. The biotech axed plans to advance into phase 3 in gastric cancer on the basis of midstage data, sending its stock down 60% to below $1, but it is forging ahead in another indication.

Tris builds clinical case for opioid alternative by showing its pain drug is less likely to be abused

Having shown last week that its opioid alternative can reduce post-surgery pain, Tris Pharma is back with another slice of clinical data to show that the drug is less likely to be abused.

UPDATED: Cell therapy biotech Aurion eyes IPO despite legal pushback from investor

Cell therapy biotech Aurion is moving forward with plans to IPO despite a pending lawsuit from one of its existing investors.

Longtime manufacturer ITM's lead radiotherapy outperforms standard of care in phase 3 neuroendocrine tumor trial

After 20 years of building radioisotope expertise as a manufacturer and supplier, German firm ITM Isotope Technologies is ready to take center stage with drugs of its own. ITM’s lead radiopharmaceutical outperformed the current standard-of-care treatment at prolonging progression-free survival in a phase 3 trial in patients with inoperable neuroendocrine tumors, the company said.

Takeda regains home rights to phase 3-stage depression drug from Neurocrine

Takeda is taking back the home license for a phase 3-stage depression drug as part of an amendment to its multi-asset collaboration with Neurocrine.

How Trump's DEI executive orders could impact healthcare

Healthcare organizations should review their DEI practices, lawyers said, and stay apprised of any enforcement actions on protecting single sex spaces. The private sector also has an opportunity to double down on its efforts to protect healthcare access, experts say.

No deal: Sage rejects Biogen's buyout offer, scouts for strategic alternatives

The company's board of directors unanimously rejected partner Biogen's $469 million buyout proposal, finding that it "significantly undervalues" the company and is not in the best interest of shareholders.

FDA's diagnostics CMO named interim agency commissioner

The FDA has tapped Sara Brenner to serve as acting commissioner as it awaits new leadership from the Trump administration to complete the congressional confirmation process.

Pfizer avoids board nominations from Starboard as proxy fight rolls on: Bloomberg

Activist Investor Starboard Value stopped short of nominating any directors to Pfizer’s board ahead of a Jan. 25 deadline, Bloomberg reported Monday. A Starboard-backed director—or two—would have given the investor more leverage as it attempts to influence Pfizer’s turnaround strategy.
 
Fierce podcasts

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Recapping the 2025 J.P. Morgan Healthcare Conference

This week on “The Top Line,” we break down the biggest stories out of JPM, from J&J’s blockbuster acquisition of Intra-Cellular Therapies to former First Lady Jill Biden’s appearance at Fierce JPM Week.
 

Resources

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Communicating the Value of Biopharma Assets to Potential Investors

How can an emerging company attract the right partner for a therapeutic asset (& optimize its value in a transaction)? This paper offers some insights.

 

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