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BioWorld - Tuesday, December 16, 2025
Home » Topics » Regulatory » IND

IND
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Antibody-drug conjugate illustration
Immuno-oncology

HLX-43, a next-generation PD-L1-targeting antibody-drug conjugate

Oct. 27, 2023
There is a need for new agents targeting PD-1/PD-L1 because many patients either do not respond or develop resistance to treatment.
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Cancer

Mustang Bio cleared to advance MB-109 into clinic in US

Oct. 27, 2023
The FDA has accepted Mustang Bio Inc.’s IND application of MB-109 for the treatment of recurrent glioblastoma (GBM) and high-grade astrocytoma. MB-109 is a treatment regimen combining MB-101 (City of Hope-developed IL13Rα2‐targeted CAR T-cell therapy) and MB-108 (Nationwide Children’s Hospital-developed HSV-1 oncolytic virus).
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Heart and DNA
Cardiovascular

FDA clears Tenaya Therapeutics’ IND for gene therapy product candidate

Oct. 27, 2023
Tenaya Therapeutics Inc. has received clearance from the FDA of the company’s IND application to initiate clinical testing of TN-401.
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Tumor microenvironment
Immuno-oncology

Ankyra Therapeutics receives clearance in US and Canada to advance its anchored immunotherapy agent into clinical trials

Oct. 25, 2023
Ankyra Therapeutics Inc. has received approval of its IND application by the FDA and its clinical trial application (CTA) by Health Canada for its lead agent, ANK-101, a novel tumor-directed anchored immune medicine.
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Concept art for "cancer cells destroyed by oncogenic virus"
Immuno-oncology

FDA clears IND for systemic oncolytic vaccinia virus therapy ASP-1012 for solid tumors

Oct. 24, 2023
Kalivir Immunotherapeutics Inc. has announced FDA clearance of an IND application for a phase I study of ASP-1012 (formerly VET2-L2) in participants with locally advanced or metastatic solid tumors. The trial is expected to begin in the first quarter of next year.
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Diagram showing parts of the eye
Ocular

Endogena Therapeutics’ candidate for geographic atrophy receives FDA clearance to enter clinic

Oct. 24, 2023
Endogena Therapeutics Inc. has received FDA clearance of its IND application for EA-2351 for geographic atrophy, an advanced form of age-related macular degeneration (AMD).
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Streptococcus pneumoniae in lungs
Immune

Vaxcyte's 31-valent PCV candidate VAX-31 receives IND clearance for invasive pneumococcal disease

Oct. 20, 2023
Vaxcyte Inc. has received FDA clearance of its IND application for VAX-31, a 31-valent pneumococcal conjugate vaccine (PCV) candidate designed to prevent invasive pneumococcal disease.
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3D illustration demonstrating CAR T therapy
Immuno-oncology

Caribou’s allogeneic anti-CLL-1 CAR T-cell therapy CB-012 cleared to enter clinic for AML

Oct. 19, 2023
Caribou Biosciences Inc. has received FDA clearance of its IND application for CB-012, an allogeneic anti-C-type lectin-like molecule-1 (anti-CLL-1) chimeric antigen receptor (CAR) T-cell therapy. CLL-1 is highly expressed on acute myeloid leukemia (AML) cells and leukemic stem cells, but it is not expressed on hematopoietic stem cells.
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3D illustration of B-cell lymphoma
Immuno-oncology

Y-Mabs’ IND for CD38-SADA receives FDA clearance for relapsed or refractory NHL

Oct. 18, 2023
Y-Mabs Therapeutics Inc. has received FDA clearance of its IND application for CD38-SADA, the company’s second program within its SAYA Y-PRIT (Self-Assembly DisAssembly Pre-targeted Radioimmunotherapy) theranostic platform.
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Tape measure, apple on scale
Endocrine/Metabolic

FDA clears IND for GLP-1/GIP/glucagon receptor agonist for type 2 diabetes and weight management

Oct. 2, 2023
The FDA has cleared IND applications for UBT-251 injection, a long-acting triple-targeted glucagon-like peptide-1 (GLP-1)/glucose-dependent insulinotropic polypeptide (GIP)/glucagon receptor agonist developed by The United Bio-Technology (Hengqin) Co. Ltd., a wholly owned subsidiary of The United Laboratories International Holdings Ltd., for adult type 2 diabetes and for overweight or obese subjects.
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