Drugs / AH-008
last change Sep 2026 re-read 3 minutes ago

AH-008

Developed for
chemotherapy-induced neuropathy
Investigated by
AnHorn Medicines Co. Ltd.

Trials 1

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 1 NCT07697560 Jun → Sep 2026 overdue chemotherapy-induced neuropathy AnHorn Medicines Co. Ltd. Recruiting No outcome recorded

News releases announcing trial results or a regulatory action · 2

DateIssuerRelease
2026-06-26 AnHorn Medicines Co. Ltd. Regulatory 【CNA News】AH-008 Achieves Dual Regulatory Milestones with U.S. FDA IND Clearance and Taiwan CDE Index Case Designation anhornmed.com ↗
The U.S. FDA IND clearance authorizes AH-008 to advance into human clinical trials, following a comprehensive review of its preclinical pharmacology, toxicology, and manufacturing data.
2026-06-23 AnHorn Medicines Co. Ltd. Regulatory AH-008 Achieves Dual Regulatory Milestones with U.S. FDA IND Clearance and Taiwan CDE Index Case Designation anhornmed.com ↗
The U.S. FDA IND clearance authorizes AH-008 to advance into human clinical trials, following a comprehensive review of its preclinical pharmacology, toxicology, and manufacturing data.

Evidence & citations 2 cited values

Every value below carries the sentence it was read from. 1 source stands behind the page.

FieldValueCited text
Known as AH-008 ClinicalTrials.gov intervention name — accepted as the source's own label NCT07697560 ↗
Route Intravenous “AH-008 administered as a single intravenous infusion” NCT07697560 ↗