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Search / Trial NCT06171048

Study Evaluating the Pharmacokinetics of CM310 in Healthy Subjects

Launched by KEYMED BIOSCIENCES CO.LTD · Dec 6, 2023

Trial Information

Current as of August 19, 2025

Not yet recruiting

Keywords

ClinConnect Summary

This clinical trial is studying a medication called CM310 to understand how it moves and behaves in the body of healthy adults. The trial is in its early phase and will involve participants who are between 20 and 45 years old, and only males can take part. To join, people must be in good health, meaning they should not have any serious medical conditions or be taking medications within 28 days before the trial starts.

If someone is eligible and decides to participate, they will be asked to sign a consent form to confirm they understand what the study involves. During the trial, participants will receive CM310 and provide information about how their bodies process the drug. It's important to note that the study is not yet recruiting participants, so there will be more information available later about how to join if someone is interested.

Gender

MALE

Eligibility criteria

  • Inclusion Criteria:
  • 20 years ≤ age ≤ 45 years.
  • Voluntarily participate in the study and sign the ICF.
  • Have the ability to understand the study.
  • Exclusion Criteria:
  • With history of chronic or serious illness.
  • With any medication within 28 days prior to administration;
  • Plan to undergo surgery during the research period;
  • With any situations unsuitable to participate in this study.

About Keymed Biosciences Co.Ltd

Keymed Biosciences Co., Ltd. is a leading biotechnology firm dedicated to the development of innovative therapeutic solutions, particularly in the fields of oncology and autoimmune diseases. With a strong emphasis on research and development, Keymed leverages cutting-edge technologies and a highly skilled team to advance its pipeline of novel biologics and small molecule drugs. The company is committed to improving patient outcomes through rigorous clinical trials and a robust regulatory strategy, aiming to deliver safe and effective treatments to address unmet medical needs globally.

Locations

Hefei, Anhui, China

Patients applied

0 patients applied

Trial Officials

Wei Hu

Principal Investigator

The Second Hospital of Anhui Medical University

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported