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BioWorld - Wednesday, May 27, 2026
Home » Topics » Regulatory, BioWorld Science

Regulatory, BioWorld Science
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Brain cancer illustration
Cancer

Exousia’s candidate for malignant glioma gains US orphan drug status

Oct. 29, 2025
No Comments
Exousia Pro Inc.’s subsidiary, Exousia AI, has received orphan drug designation from the FDA for its exosome-based treatment for malignant glioma.
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Illustration of bacteriophage therapy
Infection

Microbiotix gains IND clearance for bacteriophage therapy MP-101

Oct. 28, 2025
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Microbiotix Co. Ltd. has obtained IND approval from the Korean Ministry of Food and Drug Safety (MFDS) for MP-101, a bacteriophage therapy for patients with acute pneumonia. A phase I study in adult patients with Pseudomonas aeruginosa-induced pneumonia is expected to enroll its first patient within the year.
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Doctor with illustration of kidneys
Nephrology

CSPC’s SYH-2061 gains clinical trial clearance in China

Oct. 27, 2025
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CSPC Pharmaceutical Group Ltd. has obtained clearance from China’s National Medical Products Administration (NMPA) to conduct clinical trials with SYH-2061 injection for the treatment of IgA nephropathy and other complement-mediated diseases.
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Light micrograph of fibrosarcoma, a type of soft tissue sarcoma
Cancer

Resolute’s RS-5 designated orphan drug for soft tissue sarcomas

Oct. 27, 2025
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Resolute Science Inc.’s RS-5 has been awarded orphan drug designation by the FDA for the treatment of soft tissue sarcomas.
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Drug R&D concept image.
Cancer

IND open for Dewpoint’s condensate modulator DPTX-3186

Oct. 22, 2025
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Dewpoint Therapeutics Inc. has announced an IND in the U.S. for DPTX-3186, a first-in-class oral condensate modulator designed to selectively disrupt oncogenic Wnt/β-catenin signaling in tumors. Dosing is set to begin before year-end in a phase I/II trial conducted in partnership with cancer centers and opinion leaders in gastric and other Wnt-driven cancers.
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Test tube, dropper
Gastrointestinal

Proqr’s AX-0810 gains European clinical trial clearance

Oct. 21, 2025
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Proqr Therapeutics NV has received clinical trial application (CTA) authorization under the EMA’s new centralized review process for a phase I study of AX-0810, which is being developed for the treatment of cholestatic diseases such as primary sclerosing cholangitis and biliary atresia.
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Immune

Moonlight’s MOON-101 for peanut allergy gains IND approval

Oct. 20, 2025
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Moonlight Therapeutics Inc.’s IND application for MOON-101 has been cleared by the FDA, paving the way for a first clinical trial in adults and children with peanut allergy.
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Immuno-oncology

Tagworks’ radioimmunoconjugate TGW-211 cleared for clinical trial

Oct. 16, 2025
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Tagworks Pharmaceuticals BV has announced approval by the Dutch regulatory authorities for a clinical trial application.
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Multiple sclerosis, neurons concept art.
Neurology/psychiatric

Tr1x’s TRX-319 cleared for clinical trial in progressive MS

Oct. 15, 2025
No Comments
Tr1x Inc. has obtained IND clearance from the FDA for TRX-319, paving the way for initiation of a phase I/IIa study in progressive multiple sclerosis (MS) early next year. TRX-319 is designed to combine targeted B-cell control with active anti-inflammatory signaling and T-cell regulation, with the goal of restoring immune balance.
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3D heart in chest
Cardiovascular

IND approval for Corventum’s drug for chemo-cardioprotection

Oct. 15, 2025
No Comments
Corventum Inc. has gained IND clearance from the FDA for CVT-130 for the prevention of anthracycline-related cardiotoxicity. In cancer patients, the use of anthracyclines as chemotherapy is effective but limited by cumulative heart damage. Protecting against this chemotherapy-induced cardiac injury could enable retreatment for patients with recurrent cancer.
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