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NCT06581640RecruitingPhase 2

Chimeric Antigen Receptor Modified T Cells Targeting BCMA for the Treatment of Relapsed/Refractory Multiple Myeloma

A Clinical Study of the Safety and Efficacy of Chimeric Antigen Receptor-modified T Cells Targeting BCMA for the Treatment of Relapsed/Refractory Multiple Myeloma

Source: ClinicalTrials.gov · Last updated 25 Sept 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

To evaluate the safety and tolerability of chimeric antigen receptor gene-modified T cells targeting BCMA for the treatment of relapsed/refractory multiple myeloma

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
5 (estimated)
First submitted
30 Aug 2024
Start date
24 Sept 2024
Primary completion date
31 Dec 2028
Lead sponsor
The First Affiliated Hospital of Xiamen University
NCT number
NCT06581640

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 5
  • From 24 Sept 2024 to the primary completion date, 31 Dec 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previously received treatment targeting BCMA;
  • Underwent autologous hematopoietic stem cell transplantation within the last 6 weeks;
  • Received other experimental drug treatments within the last 3 months;

Other illness

  • Positive virology tests for hepatitis B, hepatitis C, HIV, syphilis, or cytomegalovirus;
  • History of other tumors (except for those with skin or cervical in situ cancers that have been cured by radical treatment and show no evidence of disease activity);
  • Presence of uncontrolled active bacterial or fungal infection;
  • Allergic to research-related drugs or cell components;
  • Presence of active autoimmune diseases;
  • Currently have unstable or active ulcers or gastrointestinal bleeding;
  • Unable to cooperate with treatment and efficacy evaluation due to mental or psychological disorders;

Other

  • Pregnant or nursing women, as well as women planning to become pregnant within the next six months;
  • The researcher believes that for other reasons, the individual is not suitable for the clinical trial.

Who the study is looking for

  • Age 18-80 years, no gender restrictions;
  • Diagnosed with refractory/relapsed multiple myeloma through physical examination, pathological examination, laboratory tests, and imaging studies;
  • Flow cytometry or histology confirms positive BCMA expression in myeloma cells;
  • As judged by the investigator, the expected survival time is \>3 months;
  • ECOG performance status score ≤2, KPS \>60%;
  • The patient has good liver, kidney, heart, and lung function: ALT and AST ≤2.5×ULN, those with liver involvement can be relaxed to ≤5×ULN; serum total bilirubin \<34 μmol/L; creatinine clearance rate \>30 mL/min; heart ejection fraction (EF) ≥40%, no pericardial effusion and significant arrhythmia; indoor SpO2 ≥92%;
  • Peripheral blood lymphocyte absolute count ALC ≥0.5 ×10\^9/L, PLT \>30×10\^9/L, Hb \>80 g/L and has a single collection venous access, and there are no other contraindications for hematopoietic cell separation;
  • Those with fertility must agree to use highly effective contraceptive methods;
  • The subject or their legal guardian can understand and is willing to sign a written informed consent form voluntarily.

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
The First Affiliated hospital of Xiamen University
Coordinator of this site? Confirm its status
XiamenChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.