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BioWorld - Thursday, April 9, 2026
Home » Topics » Regulatory, BioWorld Science

Regulatory, BioWorld Science
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Cardiovascular

Arrowhead seeks clinical trial clearance for ARO-DIMER-PA

Oct. 8, 2025
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Arrowhead Pharmaceuticals Inc. has filed for regulatory clearance in New Zealand.
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Colorful illustration of the heart
Cardiovascular

IND clearance for UCLA’s AD-NP1 for heart tissue regeneration

Oct. 7, 2025
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The FDA has cleared AD-NP1, a drug developed by University of California, Los Angeles (UCLA) for heart tissue regeneration, to enter clinical trials. The monoclonal antibody blocks the production of ENPP1 protein, which was found to interfere with healing after a heart attack.
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Neurology/psychiatric

FOXG1 Research Foundation’s FRF-001 designated orphan drug

Oct. 1, 2025
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The FDA has granted orphan drug designation to FRF-001, the FOXG1 Research Foundation’s lead gene therapy candidate for the treatment of FOXG1 syndrome. This follows the FDA’s earlier award of rare pediatric disease designation to the investigational therapy.
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Lab glassware and scientist
Cardiovascular

China’s NMPA clears CSPC’s SYH-2070 for clinical trials

Oct. 1, 2025
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CSPC Pharmaceutical Group Ltd. has obtained clearance from China’s National Medical Products Administration (NMPA) to conduct clinical trials in China with SYH-2070 injection, a double-stranded small interfering RNA (siRNA) drug for the treatment of hypertriglyceridemia or mixed hyperlipidemia.
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Art concept for tumor
Immuno-oncology

Simcere Zaiming’s SIM-0609 gains IND clearance for solid tumors

Sep. 29, 2025
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Simcere Zaiming Pharmaceutical Co. Ltd. has obtained IND clearance by the FDA for SIM-0609, a CDH17-targeting antibody-drug conjugate (ADC) for the treatment of advanced solid tumors. An IND was also approved in China earlier this month.
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Drug design, drug delivery & technologies

NIH launches new center to replace animal testing with organoids

Sep. 26, 2025
By Karen Carey
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About five months after the U.S. FDA disclosed its roadmap to move away from animal testing in favor of new approaches for biopharma drug development, the U.S. National Institutes of Health (NIH) said it is awarding $87 million in contracts over three years to launch the Standardized Organoid Modeling Center.
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Neurology/psychiatric

Cure Rare Disease’s CRD-003 designated orphan drug for LGMD2i/R9

Sep. 25, 2025
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The FDA has awarded orphan drug designation to Cure Rare Disease’s CRD-003 for the treatment of limb-girdle muscular dystrophy type R9 (LGMD2i/R9), a congenital muscular dystrophy caused by biallelic mutations in the FKRP gene.
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Test tubes, dropper
Dermatologic

Resvita Bio holds pre-IND meeting for RVB-003

Sep. 25, 2025
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Resvita Bio Inc. has held a pre-IND meeting with the FDA for RVB-003, its lead investigational therapy for Netherton syndrome. The FDA’s feedback gives the company a pathway to submit an IND for RVB-003 in the first half of next year, with a clinical efficacy read-out anticipated by early 2027.
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Gloved hands holding mRNA vaccine vial
Immune

GC Biopharma files Korean IND for COVID-19 mRNA vaccine

Sep. 23, 2025
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GC Biopharma Corp. has filed an IND application with the South Korean Ministry of Food and Drug Safety (MFDS) for a phase I trial of GC-4006A, an mRNA vaccine candidate for COVID-19.
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Immune

Leads Biolabs’ LBL-047 gains IND approval for autoimmune diseases

Sep. 22, 2025
No Comments
Nanjing Leads Biolabs Co. Ltd. has received IND approval from the FDA for LBL-047, its first autoimmune therapeutic candidate to enter the clinic.
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