Early Phase 1 Myeloma Trial, Recruiting NCT05093335 Sponsor: Memorial Sloan Kettering Cancer Center Condition: Myeloma
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Early Phase 1 Myeloma Trial, Recruiting

NCT05093335
Recruiting Early Phase 1

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 have been diagnosed with a slow-growing B-cell or T-cell blood cancer called Non-Hodgkin lymphoma (including lymphomas affecting the skin), or a type of Non-Hodgkin lymphoma with a variable course such as mantle cell lymphoma, with measurable signs of disease
  • People diagnosed with certain rare conditions involving abnormal immune or histiocyte cells, specifically Langerhans cell histiocytosis (LCH), Erdheim-Chester disease (ECD), or Rosai-Dorfman disease (RDD) (confirm with trial site)
  • People diagnosed with MGUS, smouldering multiple myeloma, or multiple myeloma as defined by international guidelines (confirm with trial site)
  • People diagnosed with certain solid tumours, such as lung cancer, meningioma, adrenal gland tumours including cortisol-producing growths, or cases where a tumour is strongly suspected, such as in Cushing's disease
  • People whose cancer is newly diagnosed and untreated, has not responded to previous treatment, or has come back after treatment
  • People aged 18 or older
  • Women of childbearing potential who have a negative pregnancy test from a blood sample taken within 2 weeks before joining the study, or a negative urine pregnancy test on the day of the procedure
  • People who are patients at Memorial Sloan Kettering Cancer Center (MSKCC)

Who may not be able to join:

  • People who are currently breastfeeding
  • People with a history of serious kidney problems, specifically chronic kidney disease where kidney function (eGFR) is measured at below 30 (confirm with trial site)
  • People who are unable or unwilling to undergo the scanning procedure, for example due to claustrophobia

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
Early Phase 1 studies are small, early exploratory studies that come before the main Phase 1 to 3 testing, so a standard phase success rate does not apply.

Contact this trial

Principal Investigator: Anton Nosov, MD, Memorial Sloan Kettering Cancer Center

Phone: 212-639-8575

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
Early Phase 1
Registry
ClinicalTrials.gov
Start date
1 October 2021
Est. completion
1 October 2027

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Tumor standard uptake value (SUV)

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