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BioWorld - Thursday, June 18, 2026
Home » Topics » Regulatory

Regulatory
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Illustration of cancer cells entering the blood stream
Cancer

Bryet’s ML-016 gains clearance for first-in-human trial

Oct. 8, 2025
No Comments
Bryet US Inc. has received Australian Human Research Ethics Committee (HREC) approval for its first-in-human study of ML-016 for patients with advanced cancer with lung and/or liver involvement. Enrollment in the phase I/II trial will begin early next year.
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Eye, DNA double helix illustration.
Ocular

Complement Therapeutics’ CTx-001 gains IND clearance

Oct. 8, 2025
No Comments
Complement Therapeutics GmbH has obtained clearance for CTx-001, a gene therapy candidate.
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Cardiovascular

Arrowhead seeks clinical trial clearance for ARO-DIMER-PA

Oct. 8, 2025
No Comments
Arrowhead Pharmaceuticals Inc. has filed for regulatory clearance in New Zealand.
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U.S. flag on columned building

J&J escapes $20M infringement award

Oct. 7, 2025
By Mari Serebrov
Johnson & Johnson Medtech won out over a jury verdict that found the company’s Depuy Synthes liable for $20 million for infringing a patent claimed by Rasmussen Instruments LLC.
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Vaccine vial and syringe

Latest ACIP recommendations added to CDC vaccine schedules

Oct. 7, 2025
By Mari Serebrov
No Comments
Even though the U.S. CDC is operating on a skeleton crew due to the partial government shutdown, it is updating its immunization schedules to adopt the COVID-19 and chickenpox vaccine recommendations the Advisory Committee on Immunization Practices (ACIP) made at its September meeting.
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Fiasp

IRA forecloses Novo Nordisk challenge to Medicare negotiations

Oct. 7, 2025
By Mari Serebrov
No Comments
Like the federal district court before it, the U.S. Court of Appeals for the Third Circuit said it lacks jurisdiction to rule on the merits of Novo Nordisk A/S’ claim that the CMS violated the Inflation Reduction Act (IRA) when it treated six of the company’s insulin aspart products as one negotiation-eligible single-source drug.
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IV drip

Lexeo, FDA position Friedreich ataxia therapy for accelerated path

Oct. 7, 2025
By Lee Landenberger
No Comments
Lexeo Therapeutics Inc. feels like it’s in a faster lane to a BLA for its Friedreich ataxia cardiomyopathy gene therapy after talking with the U.S. FDA. The agency told Lexeo that LX-2006 could be on the accelerated approval path if there is a mingling of the company’s data and studies.
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Colorful illustration of the heart
Cardiovascular

IND clearance for UCLA’s AD-NP1 for heart tissue regeneration

Oct. 7, 2025
No Comments
The FDA has cleared AD-NP1, a drug developed by University of California, Los Angeles (UCLA) for heart tissue regeneration, to enter clinical trials. The monoclonal antibody blocks the production of ENPP1 protein, which was found to interfere with healing after a heart attack.
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Illustration of cryoblation procedure in breast

Icecure gets FDA nod for Prosense cryoablation in breast cancer

Oct. 6, 2025
By Holland Johnson
Icecure Medical Ltd. reported that the U.S. FDA has granted marketing authorization to Icecure's de novo application for the Prosense cryoablation system for the local treatment of breast cancer in patients 70 years of age or older with biologically low-risk tumors. The authorized indication includes patients that are not suitable for surgery for breast cancer treatment.
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Decorative scales of justice in a courtroom

US Fed Circuit hands Stryker a win over PTAB

Oct. 6, 2025
By Mari Serebrov
While the final word has yet to be written, Stryker Corp. came out the biggest winner in a dispute involving four related patents owned by Osteomed LLC, part of Colson Associates’ Acumed.
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