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BioWorld - Friday, April 24, 2026
Home » Topics » FDA, BioWorld Science

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Illustration demonstrating muscle contraction in amyotrophic lateral sclerosis.
Neurology/Psychiatric

Akava announces IND clearance for AKV-9 to enter clinic for ALS

Aug. 23, 2023
Akava Therapeutics Inc. has announced FDA clearance of its IND application for AKV-9 (formerly NU-9) for the treatment of amyotrophic lateral sclerosis (ALS). The company is planning a first-in-human phase I study in healthy subjects.
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Immuno-oncology

Vincerx's antibody-drug conjugate VIP-943 receives FDA clearance for phase I study in AML

Aug. 23, 2023
Vincerx Pharma Inc. has received IND clearance from the FDA to initiate a phase I trial for VIP-943, an antibody-drug conjugate (ADC) for acute...
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Pancreatic cancer cells.
Immuno-oncology

FDA awards orphan drug designation to Canariabio's MAb-AR20.5 for pancreatic cancer

Aug. 22, 2023
Canariabio Inc.'s MAb-AR20.5 has been awarded orphan drug designation by the FDA for pancreatic cancer. MAb-AR20.5 is an IgG1k type murine monoclonal antibody that binds specifically to the circulating and tumor-associated antigen (MUC1) expressed on pancreatic cancer cells.
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Art concept for tumor
Cancer

Polϴ helicase inhibitor GSK-101 cleared by FDA for first-in-human trials with niraparib

Aug. 22, 2023
Ideaya Biosciences Inc. has announced FDA clearance of an IND for a GSK-sponsored phase I/II trial of GSK-101 (IDE-705), a small-molecule inhibitor of Polϴ helicase, in combination with GSK's PARP inhibitor niraparib tosylate monohydrate for the treatment of tumors with BRCA or other homologous recombination mutations or homologous recombination deficiency.
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Immuno-oncology

BITT's TNFR2 antibody BITT-2101 receives FDA clearance to enter clinic for NHL

Aug. 21, 2023
Boston Immune Technologies and Therapeutics Inc. (BITT) has received IND clearance from the FDA for a first-in-human trial of BITT-2101, a monoclonal antibody that targets tumor necrosis factor receptor 2 (TNFR2), in patients with relapsed or refractory non-Hodgkin lymphomas (NHLs).
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Liver anatomy illustration
Cancer

Nuvectis Pharma's NXP-800 granted orphan drug designation for cholangiocarcinoma

Aug. 18, 2023
The FDA has granted orphan drug designation to Nuvectis Pharma Inc.'s NXP-800 for the treatment of cholangiocarcinoma.
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Antibodies attacking cancer cell
Immuno-oncology

Novarock's bispecific antibody NBL-028 cleared to enter clinic for CLDN6-expressing tumors

Aug. 18, 2023
Novarock Biotherapeutics Ltd., a subsidiary of CSPC Pharmaceutical Group Ltd., has received FDA approval of its IND application for NBL-028, a CLDN6-CD137 bispecific antibody.
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Antibody-drug conjugate illustration
Immuno-oncology

Oncusp's CDH6-targeting ADC CUSP-06 cleared to enter clinic for solid tumors

Aug. 17, 2023
Oncusp Therapeutics Inc. has received IND clearance from the FDA to begin clinical trials with CUSP-06, a cadherin-6 (CDH6)-targeting antibody-drug conjugate designed for the treatment of multiple solid tumors. CDH6 is overexpressed in cancers including ovarian, renal, uterine, thyroid, lung, and cholangiocarcinoma. A phase I trial will pave the way for expansion in patients with platinum-refractory/resistant ovarian cancer and other advanced solid tumors.
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Human natural killer cell
Immune

FDA clears IND for Artiva's NK cell therapy candidate Allonk to be studied with rituximab for SLE

Aug. 17, 2023
Artiva Biotherapeutics Inc. has received FDA clearance of its IND application for Allonk (AB-101), to be used in combination with rituximab for treatment of systemic lupus erythematosus (SLE) in patients with active lupus nephritis.
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Anatomy illustration of thyroid, tumor, cancer cells
Cancer

Thryv's THRV-1257 cleared by FDA to enter clinic for anaplastic thyroid cancer

Aug. 17, 2023
Thryv Therapeutics Inc. has received FDA clearance of its IND application for THRV-1257 (THRYV-1257) for the treatment of advanced...
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