Phase 1 Myeloma Trial, Recruiting NCT06435910 Sponsor: Shenzhen Geno-Immune Medical Institute Condition: Myeloma
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Phase 1 Myeloma Trial, Recruiting

NCT06435910
Recruiting Phase 1

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 have been diagnosed with multiple myeloma or plasmacytoma (types of blood cancer)
  • People whose cancer has responded very well or completely to previous combination treatments
  • People whose doctors expect them to survive for more than 12 weeks
  • People who have suitable veins for blood draws or a procedure to collect blood cells (apheresis), and no medical reasons preventing blood withdrawal
  • People who are willing to give their informed consent and to attend follow-up appointments

Who may not be able to join:

  • Women who are pregnant or currently breastfeeding
  • People who have an active infection that is not under control
  • People who have HIV, or an active hepatitis B or hepatitis C infection
  • People who are currently taking steroid medicines in tablet or injection form (note: steroid inhalers, such as those used for asthma, are not a reason for exclusion)

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 12 July 2026
Phase 1: approximately ~10% 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

Phone: +86 0755-86573763

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 1
Sponsor
Shenzhen Geno-Immune Medical Institute
Registry
ClinicalTrials.gov
Start date
11 May 2024
Est. completion
11 July 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Safety of DC injection

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: 12 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