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BioWorld - Wednesday, June 3, 2026
Home » Topics » Regulatory » IND

IND
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Coronavirus, mRNA and syringe
Infection

Greenlight cleared to begin first-in-human study of mRNA COVID-19 vaccine candidate GLB-COV2-043

Feb. 2, 2023
Greenlight Biosciences Holdings PBC has received regulatory approval from the Rwanda Food and Drugs Authority (Rwanda FDA) to start a first-in-human phase I/II trial of its mRNA vaccine candidate against COVID-19, GLB-COV2-043, as a booster for previously vaccinated individuals.
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Gastrointestinal system with ulcerative colitis.
Gastrointestinal

Rise Therapeutics to advance R-3750 immunotherapy for ulcerative colitis

Feb. 1, 2023
Rise Therapeutics LLC has received FDA clearance for its IND application to proceed with a phase I trial of R-3750, a synthetic biology-based cellular immunotherapy being developed for the treatment of inflammatory bowel disease. The phase I trial will enroll patients with mild to moderate ulcerative.
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The epidermal growth factor receptor in the inactive (left) and active (right) form.
Immuno-oncology

Deka's IND for DK-210 (EGFR) in advanced solid cancer receives FDA clearance

Jan. 31, 2023
Deka Biosciences Inc.'s IND application has been cleared by the FDA allowing the company to proceed with a phase I trial of DK-210 (EGFR) in patients with advanced solid cancer overexpressing epidermal growth factor receptors (EGFR).
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3D heart in chest
Cardiovascular

China's CDE clears IND for Help's iPS cell-derived cardiomyocyte therapy for ischemic heart failure

Jan. 31, 2023
Help Therapeutics Co. Ltd. has received IND approval from China's Center for Drug Evaluation (CDE) for HiCM-188.
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Dermatologic

Escient gains IND clearance for first-in-human study of MRGPRX2 antagonist EP-262

Jan. 30, 2023
Escient Pharmaceuticals Inc. has obtained FDA clearance of its IND application for EP-262, a first-in-class, potent, highly selective small-molecule antagonist of Mas-related G-protein coupled receptor member X2 (MRGPRX2) for mast cell-mediated disorders.
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Antibodies attacking cancer cell
Immuno-oncology

Centessa to advance conditionally tetravalent PD-L1xCD47 bispecific monoclonal antibody

Jan. 27, 2023
Centessa Pharmaceuticals plc has received clearance of its IND application from the FDA to initiate a first-in-human phase I/IIa trial of LB-101 for the treatment of solid tumors.
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Immuno-oncology

Sana receives IND clearance for CAR T-cell therapy SC-291 for B-cell malignancies

Jan. 27, 2023
Sana Biotechnology Inc. has received FDA clearance of its IND application to initiate a first-in-human study of SC-291 in patients with various B-cell malignancies. Initial clinical data from the study are expected later this year. SC-291 is a CD19-targeted allogeneic chimeric antigen receptor (CAR) T-cell therapy developed using Sana's hypoimmune platform.
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Gastrointestinal

Exegi Pharma cleared to study EXE-346 for management of IPAA patients

Jan. 27, 2023
Exegi Pharma LLC has received FDA clearance of its IND application for EXE-346, allowing the company to initiate a clinical trial to evaluate EXE-346 in the management of excessive stool frequency in patients with an ileal pouch-anal anastomosis (IPAA, J-Pouch).
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Cancer cells
Cancer

Tango's PRMT5 inhibitors receive IND clearance, orphan drug designation

Jan. 26, 2023
The FDA has cleared Tango Therapeutics Inc.'s IND application for TNG-462, a next-generation methylthioadenosine-cooperative (MTA) inhibitor of protein arginine methyl transferase 5 (PRMT5) for the treatment of cancers with methylthioadenosine phosphorylase (MTAP) deletion.
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Cancer cell targeted in crosshairs
Immuno-oncology

FDA approves Tscan's INDs for T-Plex and MAGE-targeting TCR-T products

Jan. 25, 2023
Tscan Therapeutics Inc. has received FDA clearance of its IND applications for T-Plex, TSC-204-A0201 and TSC-204-C0702.
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