ZKLJ02
/ KumMing Longjin Pharmaceutical
- LARVOL DELTA
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January 31, 2026
A randomized, double-blind, placebo-controlled, dose-escalation Phase I clinical study to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of single intravenous administration of ZKLJ02 injection in healthy Chinese research participants
(ChiCTR)
- P=N/A | N=50 | Recruiting | Sponsor: Bishan People's Hospital of Chongqing; Yunnan Zhongke Longjin Biotechnology Co.,Ltd.
New trial • Cardiovascular • Ischemic stroke
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