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OncoMatch/Clinical Trials/NCT06185751

Safety and Efficacy of CS1 CAR-T (WS-CART-CS1) in Subjects With Multiple Myeloma

Is NCT06185751 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies multiple treatments including WS-CART-CS1 and Lymphodepleting chemotherapy for multiple myeloma.

Phase 1RecruitingWashington University School of MedicineNCT06185751Data as of May 2026

Treatment: WS-CART-CS1 · Lymphodepleting chemotherapyDespite recent therapeutic advances, multiple myeloma (MM) remains an incurable disease. Although survival has improved, there are nevertheless diminishing durations of response to each subsequent line of therapy. This highlights the need for further therapeutic innovation. BCMA-targeting CAR-T cells show impressive response rates; however, their median duration of response is disappointing. The investigators propose that CS1(SLAMF7)-targeting CAR-T cells will fill a gap in the MM armamentarium. CS1 is an attractive target in MM because it is expressed in most patients. Elotuzumab (Empliciti®), an approved anti-CS1 antibody, has proven the clinical efficacy of this target. CAR-T cells are an ideal modality to target CS1, given that two approved treatments, ide-cel (idecabtagene vicleucel, AbecmaTM) and cilta-cel (ciltacabtagene autoleucel, Carvykti™), have proven the potential for cellular immunotherapy in MM. The investigators are testing the safety and preliminary anti-myeloma efficacy of WS-CART-CS1, a CAR-T cell therapy targeting CS1.

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Extracted eligibility criteria

Cancer type

Multiple Myeloma

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Min 3 prior lines

Must have received: proteasome inhibitor (bortezomib, carfilzomib)

including proteasome inhibitor (e.g. bortezomib or carfilzomib)

Must have received: anti-CD38 therapy (daratumumab)

anti-CD38 therapy (e.g. daratumumab)

Must have received: anti-BCMA therapy (BCMA bispecific antibodies, BCMA CAR-T)

anti-BCMA therapies (e.g. BCMA bispecific antibodies or BCMA CAR-T)

Cannot have received: systemic therapy

Any prior systemic therapy for multiple myeloma within 14 days before planned day of leukapheresis

Cannot have received: cellular therapy

Receipt of any cellular therapy within 8 weeks prior to the planned start of conditioning

Lab requirements

Kidney function

calculated creatinine clearance ≥ 50 mL/min/1.73 m2 OR radioisotope glomerular filtration rate ≥ 50 mL/min/1.73 m2 OR normal serum creatinine based on age/gender per institutional normal range

Liver function

ALT (SGPT) ≤ 5 x ULN for age; Total bilirubin ≤ 2.0 x IULN (unless the patient has Grade 1 bilirubin elevation due to Gilbert's disease or a similar syndrome involving slow conjugation of bilirubin)

Cardiac function

LVEF ≥ 45% confirmed by echocardiogram or MUGA within 28 days of screening

Adequate renal, hepatic, respiratory, and cardiovascular function, as defined below

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • Washington University School of Medicine · St Louis, Missouri

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

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