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BioWorld - Friday, June 19, 2026
Home » Topics » Regulatory, BioWorld Science

Regulatory, BioWorld Science
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3D illustration demonstrating antibody-drug conjugate.
Immuno-oncology

Adcentrx’s ADC targeting Nectin-4 receives FDA clearance to enter clinic

July 18, 2023
Adcentrx Therapeutics Inc. has received FDA clearance of its IND application for ADRX-0706 for the treatment of select advanced solid tumors.
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Lab mouse
Drug design, drug delivery & technologies

US spending bill spares animals in preclinical drug development

Dec. 30, 2022
By Mari Serebrov
Tucked into the 4,155-page, $1.7 trillion spending bill for fiscal 2023 that U.S. President Joe Biden signed into law Dec. 23 is a small provision that may have outsized impact on future biosimilar and other drug development. Championed by lawmakers on both sides of the political spectrum, the provision modernizes the data that can be used to support drug development, including alternatives to animal studies.
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Infection

Ascletis files IND application for ASC-10 as treatment of monkeypox virus infection

Oct. 27, 2022
Ascletis Pharma Inc. announces that the company has filed an IND application with the FDA for ASC-10, an oral antiviral drug candidate targeting viral polymerase of monkeypox virus.
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Non-Hodgkin lymphoma cells in the blood flow
Cancer

Innocare Pharma cleared to begin clinical trials in China with BCL2 inhibitor ICP-248

Sep. 13, 2022
Innocare Pharma Ltd. has received IND approval from China's National Medical Products Administration (NMPA) to begin clinical trials of its B-cell lymphoma-2 (BCL2) inhibitor ICP-248.
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Man holding hand up to ear
Ear, Nose and Throat

Sensorion receives positive opinion on EU orphan drug designation for OTOF-GT for hearing loss

Sep. 13, 2022
The EMA's Committee for Orphan Medicinal Products (COMP) has adopted a positive opinion on Sensorion SA's application seeking orphan drug designation for OTOF-GT, a gene therapy intended for the treatment of otoferlin gene-mediated hearing loss.
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Drug vial and syringe
Neurology/Psychiatric

CSPC Pharmaceutical cleared to begin clinical trials in China of TG-103 for Alzheimer's and NASH

Sep. 12, 2022
China's National Medical Products Administration (NMPA) has cleared CSPC Pharmaceutical Group Limited to conduct clinical trials of TG-103 injection for the treatment of Alzheimer's disease and for the treatment of nonalcoholic steatohepatitis (NASH).
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Cardiovascular

Tenaya cleared to begin clinical testing of TN-301 for HFpEF

Sep. 7, 2022
Tenaya Therapeutics Inc. has received FDA clearance of its IND application to begin clinical testing of TN-301, a highly selective small-molecule inhibitor of histone deacetylase 6 (HDAC6) initially being developed for heart failure with preserved ejection fraction (HFpEF).
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Cancer cell destruction by nanoparticles
Cancer

Monte Rosa receives IND clearance for molecular glue degrader MRT-2359 for MYC-driven solid tumors

Sep. 7, 2022
Monte Rosa Therapeutics Inc. has received FDA clearance of its IND application for MRT-2359, a potent and selective GSPT1-directed molecular glue degrader (MGD).
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Test tubes, capsules, dropper
Cancer

Cancer Immuneering submits IND application for IMM-1-104 for advanced RAS-mutant solid tumors

Sep. 5, 2022
Immuneering Corp. has submitted an IND application to the FDA to support a phase I/IIa trial of IMM-1-104, an oral once-daily small molecule in development for the treatment of advanced RAS-mutant solid tumors.
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Immune

Stemcyte cleared to study umbilical cord blood stem cell therapy for post-COVID syndrome

Aug. 30, 2022
Stemcyte Inc. has received IND approval from the FDA for a phase II trial using umbilical cord blood stem cell therapy for post-COVID syndrome, or long COVID.
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