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BioWorld - Friday, May 8, 2026
Home » Topics » Regulatory, BioWorld Science

Regulatory, BioWorld Science
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Endocrine/Metabolic

CSPC Pharmaceutical’s SYH-2053 receives NMPA clearance for clinical studies in China

Nov. 30, 2023
CSPC Pharmaceutical Group Ltd.’s SYH-2053 injection has obtained clearance from China’s National Medical Products Administration (NMPA) to enter clinical trials in China.
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3D illustration of cancer in crosshairs
Cancer

Pasithea Therapeutics eyes IND filing for MEK1/2 inhibitor PAS-004 following FDA guidance

Nov. 30, 2023
Pasithea Therapeutics Corp. has received written responses from the FDA to questions submitted for a type 2 pre-IND meeting regarding the clinical development plan for PAS-004 (CIP-137401).
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Microenvironment of a HER2-expressing breast tumor
Immuno-oncology

Carisma's HER2-targeting CT-0525 cleared to enter clinic

Nov. 29, 2023
Carisma Therapeutics Inc. has received FDA clearance of its IND application for CT-0525, an ex vivo gene-modified autologous chimeric antigen receptor (CAR)-monocyte cellular therapy intended to treat solid tumors that overexpress human epidermal growth factor receptor 2 (HER2).
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Bloodstream with red and white blood cells and platelets
Hematologic

Sernova’s hemophilia cell therapy program awarded US orphan drug designation

Nov. 28, 2023
Sernova Corp. has announced that its hemophilia A program, combining the Sernova Cell Pouch with a patient’s own cells corrected for the production of factor VIII (FVIII), has been awarded U.S. orphan drug and rare pediatric disease designations.
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Infection

Ethris gains clearance for phase I study of ETH-47 for respiratory viral infections

Nov. 28, 2023
Ethris GmbH has received approval from the U.K. Medicines and Healthcare products Regulatory Agency (MHRA) to proceed with a first-in-human trial of its inhaled mRNA program, ETH-47, in healthy participants for the treatment and prophylaxis of respiratory viral infections.
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Cancer

CSPC Pharmaceutical’s SOS-1 inhibitor cleared to enter clinic in China for solid tumors

Nov. 28, 2023
CSPC Pharmaceutical Group Ltd.’s selective son of sevenless homolog 1 (SOS-1) inhibitor SYH-2038 has received clearance by China’s National Medical Products Administration (NMPA) to enter clinical trials in China.
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Silhouettes
Neurology/Psychiatric

Neumora’s M4 receptor positive allosteric modulator enters clinic for schizophrenia

Nov. 27, 2023
Neumora Therapeutics Inc. has announced IND clearance and initiation of a phase I study of NMRA-266 in healthy adults.
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Antibody-drug conjugate
Immuno-oncology

Henlius’ EGFR-targeting ADC receives FDA clearance to enter clinic for solid tumors

Nov. 24, 2023
Shanghai Henlius Biotech Inc. has announced IND approval by the FDA for HLX-42 for injection, an antibody-drug conjugate (ADC) developed under a collaboration between Henlius and Medilink Therapeutics.
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Cross section illustration of HIV virus parts
HIV/AIDS

Arenaviral therapeutic vaccine HB-500 gets IND clearance for HIV

Nov. 21, 2023
Hookipa Pharma Inc. has received clearance from the FDA for its IND application for HB-500, a novel arenaviral therapeutic vaccine for the treatment of HIV.
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Substance Use & Poisoning

NT-I7 awarded US orphan drug designation for radiation poisoning

Nov. 21, 2023
The FDA has awarded orphan drug designation to Neoimmunetech Inc.'s NT-I7 (efineptakin alfa, rhIL-7-hyFc) for the treatment of acute radiation syndrome (ARS). NT-I7, a novel long-acting recombinant human IL-7, has the potential to rapidly recover and improve the immune response following a high dose of radiation exposure.
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