Phase 3 Myeloma Trial, Recruiting NCT06508983 Sponsor: Hangzhou Sumgen Biotech Co., Ltd. Condition: Myeloma
Back to Myeloma

Phase 3 Myeloma Trial, Recruiting

NCT06508983
Recruiting Phase 3

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 able to understand and sign a consent form agreeing to take part in the study.
  • People aged between 18 and 75 years old (inclusive).
  • People whose general physical functioning falls within an acceptable range, as measured by a standard medical scoring system (a score of 0, 1, or 2 on the ECOG scale — confirm with trial site).
  • People with an expected survival of at least 3 months.
  • People who have a confirmed diagnosis of multiple myeloma with disease that can be measured and tracked during the trial.
  • People who have already had at least one previous treatment for multiple myeloma, which must have included both lenalidomide and a specific type of drug called a proteasome inhibitor (such as bortezomib, carfilzomib, or ixazomib), either separately or together.
  • People whose multiple myeloma has shown signs of getting worse during or after their most recent treatment.
  • People whose liver, kidneys, heart, and other vital organs are functioning at an adequate level.
  • Women who could become pregnant must agree to use contraception for 4 weeks before starting the trial, throughout the trial, and for 6 months after stopping the study drug SG301 or 4 weeks after stopping pomalidomide (whichever is longer), and must have two negative pregnancy tests before starting treatment.

Who may not be able to join:

  • People whose multiple myeloma never responded to any treatment at all (called "primary refractory" disease).
  • People whose myeloma has spread outside the bone marrow in a way that is not connected to the bone (confirm with trial site).
  • People whose myeloma did not respond to a previous treatment involving a type of drug called a CD38 monoclonal antibody (such as daratumumab).
  • People who have previously been treated with a drug called pomalidomide.
  • People who have received standard chemotherapy or certain targeted cancer medicines within 2 weeks (or within 5 half-lives of that drug, whichever comes first) before starting the trial.
  • People who have received biological cancer therapies within 4 weeks (or within 5 half-lives of that drug, whichever comes first) before starting the trial.
  • People who have taken part in another clinical trial and received an experimental treatment within 4 weeks (or within 5 half-lives, whichever comes first, but no less than 14 days) before starting this trial.
  • People with active hepatitis B or hepatitis C infection.
  • People with a known HIV infection.
  • People with active tuberculosis or a positive blood test for syphilis.
  • People with significant problems affecting major organs that do not meet the trial's health requirements.
  • People who have previously had a stem cell transplant (either from a donor or using their own cells) before joining the trial.
  • People with a known allergy to any ingredient in the study medicines.
  • People with other significant medical or mental health conditions — such as uncontrolled infections, uncontrolled diabetes, or certain lung conditions — that could interfere with the trial or pose a risk to their safety.

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 23 July 2026
Phase 3: approximately ~65% 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: +86 010-56315401

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 3
Sponsor
Hangzhou Sumgen Biotech Co., Ltd.
Registry
ClinicalTrials.gov
Start date
14 June 2024
Est. completion
31 March 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Adverse events (stage 1); Recommended stage 2 dose of SG301 (Stage 1); Progression Free Survival (Stage 2)

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: 23 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