Phase 1 Lymphoma Trial, Recruiting
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.
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
Where this trial is recruiting
Primary endpoints
Dose Limiting Toxicity (DLT)
Can't join this trial?
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.