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OncoMatch/Clinical Trials/NCT05846880

VitD3 Supplementation in Patients With Multiple Myeloma

Is NCT05846880 recruiting? Yes, currently enrolling (Jun 2026). This Early Phase 1 trial studies multiple treatments including Lenalidomide and Maintenance Vitamin D for multiple myeloma.

Early Phase 1RecruitingAmany Keruakous, MD, MS.NCT05846880Data as of Jun 2026

Treatment: Lenalidomide · Maintenance Vitamin D · No maintenance Vitamin DThe goal of this clinical trial is to evaluate post-transplant immune reconstitution and lymphocyte recovery as well as the 3-year progression-free survival of patients with multiple myeloma in two treatment arms. One arm will receive Maintenance Vitamin D and the other arm will receive no maintenance Vitamin D prior to ASCT. Post ASCT arm 1 will have lenalidomide and maintenance VitD, and arm 2 will receive lenalidomide and no maintenance VitD. This clinical trial will also evaluate the overall response rate and survival for both treatment arms.

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Extracted eligibility criteria

Treatments studied

Endocrine / hormonal

Lenalidomide

Other

Maintenance Vitamin DNo maintenance Vitamin D

Cancer type

Multiple Myeloma

Performance status

ZUBROD/ECOG 0–2

Zubrod/ECOG Performance Status  2

Prior therapy

Min 1 prior line

Must have received: systemic induction therapy — prior to ASCT

systemic induction therapy prior to ASCT

Cannot have received: allograft

Prior allograft

Cannot have received: organ transplant requiring immunosuppressive therapy

prior organ transplant requiring immunosuppressive therapy

Cannot have received: autologous stem cell transplant

have already received a previous autologous transplantation (e.g., requiring second ASCT at time of screening)

Cannot have received: investigational agent

Received any investigational agents within 14 days prior to registration

Lab requirements

Kidney function

creatinine clearance (CrCl)  10 mL/min., as measured by a 24-hour urine collection, or estimated by the Cockcroft and Gault formula

Liver function

Total bilirubin  1.5 x IULN and AST and ALT  3.0 x IULN

Patients must have evidence of adequate renal function ... CrCl  10 mL/min ... adequate hepatic function ... Total bilirubin  1.5 x IULN and AST and ALT  3.0 x IULN

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

US trial sites

  • Georgia Cancer Center at Augusta University · Augusta, Georgia

Showing up to 5 US sites.

See all sites on ClinicalTrials.gov →

Frequently asked questions

Is NCT05846880 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior allograft, organ transplant requiring immunosuppressive therapy, autologous stem cell transplant disqualifies patients from enrollment.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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