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BioWorld - Monday, February 9, 2026
Home » Topics » Regulatory, BioWorld Science

Regulatory, BioWorld Science
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Microscopic image of acute myeloid leukemia (AML) cells.
Cancer

Oral KAT2A/B degrader gets go-ahead for acute myeloid leukemia

Feb. 5, 2025
Auron Therapeutics Inc. has received FDA clearance of its IND application for its oral KAT2A/B degrader AUTX-703 in hematological malignancies. A phase I proof-of-concept trial in acute myeloid leukemia (AML) will open enrollment this quarter, supported by a recently completed $27 million series B financing.
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Hair and scalp under magnifying glass
Dermatologic

HCW-9302 gains IND clearance for first-in-human study in alopecia areata

Feb. 4, 2025
HCW Biologics Inc. has received clearance of its IND application from the FDA to initiate a first-in-human phase I trial to evaluate HCW-9302 in patients with moderate to severe alopecia areata.
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Art concept for molecular glue degradation
Cancer

Seed’s RBM39 degrader awarded US orphan drug, rare pediatric disease designations

Jan. 29, 2025
Seed Therapeutics Inc.’s ST-01156 has been awarded orphan drug designation for the treatment of Ewing sarcoma as well as rare pediatric disease designation by the FDA.
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Illustration of antibodies attacking neurons
Immune

Allogene’s ALLO-329 gains IND clearance for autoimmune diseases

Jan. 29, 2025
Allogene Therapeutics Inc. has obtained IND clearance from the FDA for a rheumatology basket study of ALLO-329.
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Colorized transmission electron micrograph of SARS-CoV-2.
Immune

Ocugen’s OCU-500 inhaled mucosal vaccine for COVID-19 gains IND clearance

Jan. 27, 2025
Ocugen Inc. has received IND clearance from the FDA for OCU-500, an inhaled mucosal vaccine for COVID-19. The National Institute of Allergy and Infectious Diseases (NIAID) will sponsor and conduct a phase I trial of OCU-500 administered via inhalation into the lungs and intranasally as a spray.
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Eye and DNA illustration
Neurology/psychiatric

Tikun programs receive orphan, rare pediatric disease designations

Jan. 23, 2025
Tikun Therapeutics Inc. has obtained U.S. orphan drug and rare pediatric disease designations for its programs in familial dysautonomia, namely its rAAV2-U1a-hELP1 gene replacement therapy for the treatment of optic neuropathy in familial dysautonomia and BPN-36964 for systemic treatment of familial dysautonomia.
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DNA illustration
Cardiovascular

Repair Biotechnologies holds pre-IND meeting with FDA for REP-003

Jan. 22, 2025
Repair Biotechnologies Inc. has received encouraging feedback from a pre-IND meeting with the FDA as it works toward an IND filing to conduct a phase Ib study of its REP-0003 mRNA therapy in patients with homozygous familial hypercholesterolemia (HoFH).
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Antibodies attacking cancer cell
Immuno-oncology

Axcynsis gains IND clearance for AT03-65 for CLDN6-positive solid tumors

Jan. 16, 2025
Axcynsis Therapeutics Pte Ltd. has gained IND clearance from the FDA for AT03-65 for the treatment of patients with CLDN6-positive solid tumors. Axcynsis is planning to initiate a phase I trial in the U.S. during the current quarter in patients with advanced CLDN6-positive solid tumors.
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Test tubes, dropper and capsules
Neurology/psychiatric

Pheno gets clinical trial clearance for remyelination therapeutic

Jan. 15, 2025
Pheno Therapeutics Ltd. has received clinical trial authorization (CTA) from the UK’s Medicines and Healthcare products Regulatory Agency (MHRA) for its lead candidate, PTD-802. The program will progress to a first-in-human phase I trial.
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Immuno-oncology art concept
Immuno-oncology

Rise Therapeutics’ R-5780 gains IND clearance from FDA

Jan. 14, 2025
Rise Therapeutics LLC has gained IND clearance from the FDA to initiate a phase I trial of R-5780 in patients with cancer.
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