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BioWorld - Saturday, February 7, 2026
Home » Topics » Regulatory » IND

IND
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Cancer

Pasithea’s macrocyclic MEK inhibitor cleared by FDA to enter clinic for advanced solid tumors

Jan. 3, 2024
Pasithea Therapeutics Corp. has received IND clearance by the FDA to evaluate PAS-004, a small-molecule allosteric inhibitor of MEK 1/2.
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Antibody-drug conjugate illustration
Immuno-oncology

Obi Pharma to advance TROP2-targeted ADC into clinic in US

Jan. 3, 2024
Obi Pharma Inc. has received FDA clearance for its IND application to conduct a phase I/II study of OBI-992, a novel antibody-drug conjugate (ADC) cancer therapy targeting TROP2. The trial will open shortly and aims to enroll patients with advanced solid tumors, including non-small-cell lung cancer, small-cell lung cancer and gastric cancer, although several other cancers are also potential targets.
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Inflammatory

Atom Bioscience’s ABP-745 cleared to enter clinic in US for acute gout

Jan. 2, 2024
Jiangsu Atom Bioscience and Pharmaceutical Co. Ltd. has received FDA clearance of its IND application for a phase I trial in the U.S. of ABP-745, an anti-inflammatory oral small-molecule drug, for the treatment of acute gout.
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Endocrine/Metabolic

Neurobo Pharmaceuticals submits IND in US for DA-1726

Dec. 29, 2023
Neurobo Pharmaceuticals Inc. has submitted an IND application to the U.S. FDA for DA-1726.
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Kidneys
Nephrology

Jemincare obtains approvals to advance five drugs into clinical trials

Dec. 28, 2023
Jiangxi Jemincare Group Co. Ltd. has reported that its wholly owned subsidiary company, Shanghai Jemincare Pharmaceutical Co. Ltd., recently received approvals for clinical trials of five of its drugs in the fields of cancer, kidney and infectious diseases.
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Photomicrograph of bone marrow aspirate showing myeloblasts of acute myeloid leukemia
Cancer

FDA clears Senti Biosciences’ IND for SENTI-202

Dec. 27, 2023
Senti Biosciences Inc. has received clearance of its IND application from the FDA for SENTI-202, an off-the-shelf chimeric antigen receptor natural killer (CAR-NK) cell therapy product candidate designed to selectively target and eliminate CD33- and/or FLT3-expressing hematologic malignancies, such as acute myeloid leukemia (AML) and myelodysplastic syndrome, while sparing healthy bone marrow cells.
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Musculoskeletal

Aurinia submits IND for AUR-200 for autoimmune diseases

Dec. 22, 2023
Aurinia Pharmaceuticals Inc. has submitted an IND application to the FDA for AUR-200, a potential next-generation therapy for B-cell-mediated autoimmune diseases.
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Cancer cell targeted in crosshairs
Immuno-oncology

Avstera’s AVS-100 cleared to enter clinic for solid tumors

Dec. 19, 2023
Avstera Therapeutics Corp. has received FDA clearance of its IND application for HDAC6 inhibitor AVS-100. Avstera intends to initiate a phase Ia/b trial in the first half of 2024 to evaluate AVS-100 alone and in combination with pembrolizumab in locally advanced or metastatic solid tumors.
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Urinary tract with kidneys, adrenalin glands, ureter and vessels on light blue background
Infection

NRX-101 receives FDA clearance to enter clinic for cUTI

Dec. 19, 2023
Nrx Pharmaceuticals Inc. has announced FDA clearance of its IND application for the use of NRX-101 (lurasidone hydrochloride/D-cycloserine) for the treatment of complicated urinary tract infections (cUTI).
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3D illustration of tumor
Cancer

Immuneering’s IMM-6-415 receives FDA clearance for phase I/IIa trial in solid tumors with RAF or RAS mutations

Dec. 13, 2023
Immuneering Corp. has obtained FDA clearance of its IND application for IMM-6-415, an oral, twice-daily small molecule in development for the treatment of advanced RAF or RAS mutant solid tumors.
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