Phase 1 Lymphoma Trial, Recruiting NCT05679895 Sponsor: OneChain Immunotherapeutics Condition: Lymphoma
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Phase 1 Lymphoma Trial, Recruiting

NCT05679895
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:

  • Children older than 2 years, or adults of any gender
  • People whose cancer cells show a specific marker called CD1a on at least 20% of the abnormal cells, confirmed by laboratory testing
  • People diagnosed with a type of blood cancer called T-cell acute lymphoblastic leukaemia or lymphoblastic lymphoma (T-ALL/LL) that has come back or has not responded to treatment — this includes people whose cancer did not go away after at least two rounds of chemotherapy, people who have had one or more relapses after standard treatment, people whose cancer came back after a bone marrow/stem cell transplant, or people whose cancer persisted after chemotherapy in a way that means a transplant is not considered suitable
  • People who are not able to have children, or people who commit to using a highly effective form of contraception throughout the study

Who may not be able to join:

  • People with serious problems affecting the heart (such as reduced heart pumping function below a certain level), lungs, liver, kidneys, or brain that are not under control
  • People who had a bone marrow/stem cell transplant less than 3 months ago, or who still need medication to manage graft-versus-host disease (a complication where transplanted cells attack the body)
  • People with uncontrolled epilepsy or a severe condition affecting the brain or nervous system
  • People with an active bacterial, fungal, or viral infection that is not being adequately controlled with treatment
  • People known to have HIV, or an active hepatitis B or hepatitis C infection
  • People who are pregnant or breastfeeding
  • People with a serious illness or medical condition that would make it unsafe to follow the trial's treatment plan
  • People with a serious autoimmune disease or a condition that significantly weakens the immune system
  • People who have taken part in another experimental drug trial within 6 weeks before the trial treatment (called OC-1) would be given
  • People with another type of cancer that is not currently under control

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

Phone: 34 93 403 58 62

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
Sponsor
OneChain Immunotherapeutics
Registry
ClinicalTrials.gov
Start date
31 January 2023
Est. completion
1 December 2027

Where this trial is recruiting

🇪🇸 Spain

Primary endpoints

Number of adverse events grade III-IV; Incidence of severe Cytokine release syndrome (CRS) and Immune effector cell-associated neurotoxicity syndrome (ICANS); Non-relapse treatment-related mortality (NRM); Number of adverse events of special interest (AESI); Assessment of the immunological homeostasis; Incidence of the treatment-related dermatological events; Number of patients developing 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