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BioWorld - Monday, December 22, 2025
Home » Topics » Regulatory, BioWorld Science

Regulatory, BioWorld Science
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Illustration of tumor
Immuno-oncology

Kalivir’s oncolytic immunotherapy VET3-TGI cleared by FDA to enter clinic for solid tumors

July 1, 2024
Kalivir Immunotherapeutics Inc. has announced FDA clearance of its IND application for VET3-TGI for patients with incurable, advanced solid tumors.
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Immuno-oncology

SCG’s HPV-specific TCR T-cell therapy SCG-142 receives IND clearance in US

July 1, 2024
SCG Cell Therapy Pte Ltd. has gained FDA clearance of its IND application to initiate a phase I/II trial of SCG-142, a novel next-generation human papillomavirus (HPV) E7-specific T-cell receptor-engineered T (TCR T)-cell therapy for patients with HPV-associated solid tumors.
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3D illustration of the cross-section of skin layers with atopic dermatitis
Dermatologic

Concerto Bioscience’s live biotherapeutic product gains IND clearance for atopic dermatitis

June 27, 2024
Concerto Bioscience Inc. has received FDA clearance of its IND application to initiate a first-in-human phase I trial of Ensemble No.2 (ENS-002), an investigational live biotherapeutic product to treat atopic dermatitis.
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Art concept for molecular glue degradation
Gastrointestinal

Monte Rosa Therapeutics files IND application for molecular glue degrader MRT-6160

June 27, 2024
Monte Rosa Therapeutics Inc. has submitted an IND application to the FDA for MRT-6160, a highly selective and orally bioavailable molecular glue degrader directed against VAV1 in development for systemic and neurological autoimmune diseases.
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Gastrointestinal

Resolution Therapeutics’ engineered macrophage cell therapy to enter clinic for decompensated liver cirrhosis

June 27, 2024
Resolution Therapeutics Ltd. has received approval from the U.K. Medicines and Healthcare products Regulatory Agency (MHRA) to initiate a phase I/II study of its lead candidate RTX-001 in patients with decompensated liver cirrhosis.
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Multiple myeloma illustration
Immuno-oncology

CSPC’s mRNA-LNP-based CAR T-cell therapy cleared to enter clinic in China for multiple myeloma

June 26, 2024
CSPC Pharmaceutical Group Ltd. has obtained clearance from China’s National Medical Products Administration (NMPA) to conduct clinical trials in China with the first mRNA-lipid nanoparticles (LNP)-based CAR T-cell injection, SYS-6020.
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CAR T cells attacking cancer cell
Immuno-oncology

Adicet’s λδ CAR T-cell therapy ADI-270 gains IND clearance for renal cell carcinoma

June 25, 2024
Adicet Bio Inc. has obtained FDA clearance of its IND application to evaluate ADI-270, an armored allogeneic λδ CAR T-cell therapy candidate targeting CD70-positive cancers, for the treatment of relapsed or refractory renal cell carcinoma (RCC).
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Close up of man's eye
Ocular

4D Molecular Therapeutics’ 4D-175 gains FDA clearance for phase I trial in geographic atrophy

June 25, 2024
4D Molecular Therapeutics Inc. has obtained IND clearance by the FDA for 4D-175, an R100 vector-based intravitreal genetic medicine, for the treatment of patients with geographic atrophy.
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Urology

EG 427 obtains IND clearance for gene therapy for neurogenic detrusor overactivity in spinal cord injury patients

June 25, 2024
EG 427 SAS has received IND clearance from the FDA for EG-110A, a gene therapy for the treatment of neurogenic detrusor overactivity in patients with spinal cord injury. A phase Ib/IIa study is being initiated.
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Microscope with laptop displaying histology image.
Cancer

Genfleet’s KRAS G12D inhibitor GFH-375 receives NMPA clearance to enter clinic in China

June 20, 2024
Genfleet Therapeutics (Shanghai) Co. Ltd. has obtained clearance from China’s National Medical Products Administration (NMPA) to advance GFH-375 (VS-7375) into a phase I/II study in patients with advanced solid tumors with KRAS G12D mutation.
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