Drugs / JMT206
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JMT206

Investigated by
Shanghai JMT-Bio Inc.

Trials 1

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 1 NCT07419698 Jan → Sep 2026 overdue — Shanghai JMT-Bio Inc. Recruiting No outcome recorded

News releases announcing trial results or a regulatory action · 2

DateIssuerRelease
2025-12-10 CSPC ZhongQi Pharmaceutical Technology Co., Ltd. Regulatory VOLUNTARY ANNOUNCEMENT - RECOMBINANT FULLY HUMAN ANTI-ACTRIIA/IIB MONOCLONAL ANTIBODY (JMT206) OBTAINS CLINICAL TRIAL APPROVAL IN THE U.S. irasia.com ↗
The Board of Directors (the ‘‘Board ’’) of CSPC Pharmaceutical Group Limited (the ‘‘Company ’’, together with its subsidiaries, the ‘‘Group ’’) is pleased to announce that the recombinant fully human anti-ActRIIA/IIB monoclonal antibody (JMT206) (the ‘‘Product ’’) developed by the Group has obtained approval from the U.S. Food and Drug Administratio n (FDA) to conduct clinical trials in the U.S.
2025-11-26 CSPC ZhongQi Pharmaceutical Technology Co., Ltd. Regulatory VOLUNTARY ANNOUNCEMENT - RECOMBINANT FULLY HUMAN ANTI-ACTRIIA/IIB MONOCLONAL ANTIBODY (JMT206) OBTAINS CLINICAL TRIAL APPROVAL IN CHINA irasia.com ↗
The Board of Directors (the ‘‘Board ’’) of CSPC Pharmaceutical Group Limited (the ‘‘Company ’’, together with its subsidiaries, the ‘‘Group ’’) is pleased to announce that the recombinant fully human anti-ActRIIA/IIB monoclonal antibody drug (JMT206) (the ‘‘Product ’’) developed by the Group has obtained approval from the National Medical Products Admin istration of the People ’s Republic of China to conduct clinical trials in China.

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 JMT206 ClinicalTrials.gov intervention name — accepted as the source's own label NCT07419698 ↗
Route Subcutaneous “Subcutaneous injection, single dose.” NCT07419698 ↗