Phase 2 Lymphoma Trial, Recruiting NCT03587844 Sponsor: Memorial Sloan Kettering Cancer Center Condition: Lymphoma
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Phase 2 Lymphoma Trial, Recruiting

NCT03587844
Recruiting Phase 2

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:

For people with Mycosis Fungoides (MF) or Sézary Syndrome (SS):

  • A confirmed diagnosis of mycosis fungoides or Sézary syndrome at the enrolling hospital, with disease at stage IB or higher (meaning patches, plaques, or papules covering at least 10% of the skin, or affecting internal organs)
  • People whose mycosis fungoides tests negative for the CD30 marker are still eligible
  • Adults aged 18 or older
  • People with a general health and activity level rated as reasonably functional (an ECOG performance score of 2 or below — confirm with trial site)
  • For Group 1 (Cohort 1): People who have never previously received the drug brentuximab vedotin
  • For Group 2 (Cohort 2): People who have previously received brentuximab vedotin for MF or SS (note: people who left Cohort 1 due to side effects are not eligible for Cohort 2)
  • Any previous cancer treatments must have been stopped at least 2 weeks before starting the trial
  • Low-dose steroid use (equivalent to no more than 10mg per day of prednisone) may be permitted in certain circumstances, after discussion with the lead doctor
  • People who are HIV-positive may be eligible if they have been on stable HIV treatment for at least 12 weeks before the trial starts, and have a CD4 cell count above 200 within 7 days of starting
  • Women who could become pregnant must be using an acceptable form of contraception as required by the institution

For people with Lymphomatoid Papulosis (LyP):

  • A confirmed diagnosis of lymphomatoid papulosis at the enrolling hospital
  • A condition that the treating doctor judges requires systemic (whole-body) treatment
  • Adults aged 18 or older
  • People with a general health and activity level rated as reasonably functional (ECOG performance score of 2 or below — confirm with trial site)
  • Any previous cancer treatments must have been stopped at least 2 weeks before starting the trial
  • Low-dose steroid use may be permitted in certain circumstances (same conditions as above)
  • People who are HIV-positive may be eligible under the same conditions described above
  • Women who could become pregnant must be using an acceptable form of contraception as required by the institution

Who may not be able to join:

  • People currently receiving other systemic (whole-body) cancer treatments for MF, SS, or LyP at the same time as this trial
  • People with moderate or severe nerve damage or nerve-related symptoms (Grade 2 or higher neuropathy — confirm with trial site)
  • People with severely reduced kidney function (confirm with trial site)
  • People with moderate or severe liver disease (confirm with trial site)
  • Women who could become pregnant must have a negative blood pregnancy test within one week of starting the trial
  • For Cohort 1 only: People who have previously received the drug brentuximab vedotin
  • People currently receiving systemic treatment for a separate, different cancer (other than T-cell lymphoma) — though some exceptions may be possible after discussion with the principal investigator
  • For Cohort 2 only: People whose MF or SS got worse while on the standard dose of brentuximab vedotin previously

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 14 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Alison Moskowitz, MD, Memorial Sloan Kettering Cancer Center

Phone: 646-608-3726

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
Phase 2
Registry
ClinicalTrials.gov
Start date
3 July 2018
Est. completion
1 July 2027

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

overall response

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: 14 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