Phase 2 Myeloma Trial, Recruiting
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 willing to follow the treatment plan and visit schedule, and who agree to sign a consent form
- People who are 18 years of age or older at the time of signing the consent form
- People whose general physical functioning is rated at a level showing they are fully active or have only minor limitations in physical activity (based on a standard medical scale called ECOG, scored 0 or 1) (confirm with trial site)
- People who have been formally diagnosed with multiple myeloma according to recognised international diagnostic guidelines
- People who are expected to live for at least 12 weeks
- People who are able to have children (including men and pre-menopausal women, or women who went through menopause less than two years ago) who are willing to use effective contraception from the time of signing the consent form until 6 months after the last dose of the trial drug — acceptable methods include abstinence, intrauterine devices, hormonal contraception, or correct condom use; women in this category must also have a negative blood pregnancy test within 7 days before starting the trial drug
Who may not be able to join:
- People who had major surgery (not including needle biopsy) or a serious injury within 4 weeks before starting the trial drug, or who are expected to need planned surgery during the trial
- People who have used certain immune-regulating medications — such as thymosin, interleukin-2, or interferon — within 14 days before starting the trial drug
- People who have used corticosteroids or other immune-suppressing medications taken throughout the whole body within 14 days before starting the trial drug (note: creams, eye drops, joint injections, nasal sprays, inhalers, or short-term use to prevent allergic reactions to contrast dye are generally not included in this restriction — confirm with trial site)
- People with currently active hepatitis B or hepatitis C infection
- People who currently have an active infection requiring intravenous (drip) antibiotic or antiviral treatment
- People with a history of immune system deficiency conditions, including those who test positive for HIV
- People who are pregnant or currently breastfeeding
- People the trial doctor considers unsuitable for the study due to other health or compliance concerns
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.
Contact this trial
Principal Investigator: Jin Lu, Peking University People's Hospital
Phone: 025-83378099
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
Where this trial is recruiting
Primary endpoints
Objective Response Rate (ORR); Dose-limiting toxicities(DLT); Maximum tolerated dose (MTD)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.