Phase 1 Lymphoma Trial, Recruiting NCT06176690 Sponsor: Baylor College of Medicine Condition: Lymphoma
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Phase 1 Lymphoma Trial, Recruiting

NCT06176690
Recruiting 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 diagnosed with one of the following: Hodgkin lymphoma, CD30-positive aggressive B-cell lymphoma, ALK-negative anaplastic T-cell lymphoma or other peripheral T-cell lymphoma, or ALK-positive anaplastic T-cell lymphoma
  • People whose tumour has tested positive for a protein called CD30, confirmed by a certified pathology laboratory
  • People aged 12 to 75 years old
  • People whose liver is functioning within acceptable levels, based on a substance called bilirubin (a different, slightly higher limit applies to those with a condition called Gilbert syndrome — confirm with trial site)
  • People whose liver enzyme levels (AST) are within an acceptable range
  • People whose kidneys are functioning at an adequate level, based on a test called estimated GFR being above 70 mL/min
  • People whose blood oxygen level is above 90% when breathing normal room air
  • People with a general health and functioning score above 60% on standard medical scales (Karnofsky or Lansky)
  • People who have recovered from the non-blood-related side effects of any previous chemotherapy
  • People who are sexually active and are willing to use effective contraception during the trial and for 6 months after it ends; male partners are also required to use a condom
  • People (or their legal guardian) who have read, understood, and signed the informed consent form

Who may not be able to join:

  • People who have received an experimental cell therapy or vaccine within the past 6 weeks
  • People who have received an experimental small molecule drug within the past 2 weeks
  • People who have received a type of treatment targeting the CD30 protein (antibody-based) within the past 4 weeks
  • People who have had an allergic reaction to products containing mouse-derived proteins
  • People who are pregnant or breastfeeding
  • People whose tumour is located in a place where any swelling could block their airway (assessed by the trial doctors)
  • People currently taking steroid medications (such as prednisone) at a daily dose of 10 mg or more
  • People with an active, serious bacterial, viral, or fungal infection that is not under control
  • People with significant heart disease causing symptoms at rest or with minimal activity (confirm with trial site)

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 13 July 2026
Phase 1: approximately ~10% 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: Premal Lulla, MD, Baylor College of Medicine

Phone: 713-441-1450

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 1
Registry
ClinicalTrials.gov
Start date
27 October 2025
Est. completion
27 July 2028

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Dose Limiting Toxicity (DLT)

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: 13 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