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ACTIVE NOT RECRUITING Phase 1

Autologous CD30.CAR-T in Combination With Nivolumab in cHL Patients After Failure of Frontline Therapy

NCT05352828 · View on ClinicalTrials.gov ↗

Study Summary

This is a Phase 1b, multicenter, open-label, single arm study to evaluate the safety and efficacy of the combination therapy, CD30.CAR-T and the programmed cell death protein-1 (PD-1) checkpoint inhibitor, nivolumab, in patients aged 12 years of age and above with relapsed or refractory classical Hodgkin lymphoma (cHL) following failure of standard frontline therapy.

Interventions

  • DRUG Fludarabine
  • DRUG Nivolumab
  • DRUG Bendamustine
  • DRUG Autologous CD30.CAR-T

Study Locations (5)

Texas

  • Baylor College of Medicine — Houston
  • MD Anderson Cancer Center — Houston

California

  • City of Hope National Medical Center — Duarte

Florida

  • University of Miami — Miami

North Carolina

  • UNC Lineberger Comprehensive Cancer Center — Chapel Hill

Trial Details

FieldValue
Enrollment Target 15 participants
Start Date 2022-07-25
Est. Completion 2037-12-15
Phase Phase 1

Sponsor

Tessa Therapeutics

3 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05352828

The ClinicalTrials.gov registry entry for NCT05352828 describes a study currently listed as active not recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 15 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Tessa Therapeutics, which has 3 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Classical Hodgkin Lymphoma appearing as the primary indexed condition, and to 4 interventions — of which Fludarabine is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT05352828 reports 5 study locations spanning 4 distinct geographic areas — top geographies include Texas, California, Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT05352828 about?

NCT05352828 is a clinical study titled "Autologous CD30.CAR-T in Combination With Nivolumab in cHL Patients After Failure of Frontline Therapy". This is a Phase 1b, multicenter, open-label, single arm study to evaluate the safety and efficacy of the combination therapy, CD30.CAR-T and the programmed cell death protein-1 (PD-1) checkpoint inhibitor, nivolumab, in patients aged 12 years of age and above with relapsed or refractory classical Ho...

What is the current status of trial NCT05352828?

This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 15 participants. The study started on 2022-07-25. Estimated completion is 2037-12-15.

What conditions does trial NCT05352828 study?

This clinical trial studies the following conditions: Classical Hodgkin Lymphoma, Hodgkin Disease Recurrent, Hodgkin Disease Refractory. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05352828?

The interventions under investigation include: Fludarabine (DRUG), Nivolumab (DRUG), Bendamustine (DRUG), Autologous CD30.CAR-T (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05352828?

This trial is sponsored by Tessa Therapeutics, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05352828 being conducted?

This trial has 5 study locations across California, Florida, North Carolina, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial