Phase 2 Lymphoma Trial, Recruiting NCT06642792 Sponsor: Akeso Condition: Lymphoma
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Phase 2 Lymphoma Trial, Recruiting

NCT06642792
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:

  • People who are 18 years of age or older at the time of joining.
  • People whose general health and ability to carry out daily activities is rated at a good to fully active level (a score of 0 or 1 on a standard oncology scale).
  • People who are expected to live for at least 12 weeks.
  • People who have been diagnosed with relapsed or refractory classical Hodgkin lymphoma (a type of blood cancer that has come back or stopped responding to treatment), confirmed using standard 2014 diagnostic guidelines.
  • People whose cancer has continued to grow or spread after receiving a type of immunotherapy drug that targets the PD-1 or PD-L1 pathway.
  • People whose liver, kidneys, and other organs are functioning well enough to meet the trial's requirements.
  • People of reproductive potential who agree to use effective contraception from the start of the screening period until 120 days after the last dose of the study treatment.

Who may not be able to join:

  • People diagnosed with a specific subtype of Hodgkin lymphoma called nodular lymphocyte-predominant Hodgkin lymphoma (NLPHL), or a related condition called gray zone lymphoma.
  • People whose lymphoma has spread to the brain or spinal cord.
  • People with a known history of a viral infection called HTLV-1 (human T-cell leukemia virus type 1).
  • People who have had a stem cell transplant using their own cells, or a specialised immune cell therapy called CAR-T, within the 90 days before the first dose of the study treatment.
  • People who have previously received a stem cell transplant or organ transplant from another person (a donor).
  • People who have previously been treated with any therapy targeting certain immune pathways called CD47-SIRPα or LAG-3.
  • People who have had another type of cancer within the 3 years before joining, or who still have signs of a cancer that was diagnosed more than 3 years ago.
  • People who have had an active autoimmune disease (where the immune system attacks the body) requiring ongoing medical treatment within the past 2 years.
  • People with a history of active inflammatory bowel disease (such as Crohn's disease or ulcerative colitis), or who have had this confirmed in the past.
  • People who have had, or currently have, a lung condition called interstitial lung disease that has required steroid treatment.
  • People with a known active Hepatitis B or Hepatitis C infection.
  • People who still have unresolved side effects from previous cancer treatments.
  • People with other serious health conditions that are not well controlled.

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 21 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: Wenting Li, MD, Akeso

Phone: +86(0760)89873999

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
Sponsor
Akeso
Registry
ClinicalTrials.gov
Start date
17 January 2025
Est. completion
1 November 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Phase I: Number of participants with dose limiting toxicity (DLT); Phase I/II: Incidence and severity of adverse events (AEs); Phase I/II: Objective response rate (ORR)

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: 21 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