Phase 2 Myeloma Trial, Recruiting NCT05299424 Sponsor: Keymed Biosciences Co.Ltd Condition: Myeloma
Back to Myeloma

Phase 2 Myeloma Trial, Recruiting

NCT05299424
Recruiting Phase 2

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who are reasonably well and able to carry out daily activities, based on a standard cancer health scale rated 0 to 2 (where 0 means fully active and 2 means limited in physically strenuous activity but able to walk and do light work).
  • People with multiple myeloma that has come back or stopped responding to treatment, who have already tried at least two different myeloma treatments — including at least one from each of these three types: a proteasome inhibitor, an immunomodulatory drug, and an anti-CD38 antibody treatment (where that treatment was available to them).

Who may not be able to join:

  • People who have previously received a treatment that targets a protein called BCMA on myeloma cells.
  • People who have previously received a type of treatment called CAR-T cell therapy.
  • People who have received any anti-cancer treatment within 3 weeks, or within 5 half-lives of that drug (whichever period is shorter), before the first dose of the trial drug CM336.

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 22 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Hongmei Jing, Peking University Third Hospital

Phone: 028-88610620

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
Keymed Biosciences Co.Ltd
Registry
ClinicalTrials.gov
Start date
9 August 2022
Est. completion
1 December 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Dose-limiting toxicities (DLTs); Adverse events (AEs); Overall Response Rate (ORR)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 22 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov