Phase 1 Lymphoma Trial, Recruiting NCT06690827 Sponsor: Chongqing Precision Biotech Co., Ltd Condition: Lymphoma
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Phase 1 Lymphoma Trial, Recruiting

NCT06690827
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:

  • Adults aged 18 to 75 years (inclusive), of any gender
  • People whose cancer cells test positive for a protein called CD123, confirmed by a laboratory blood test
  • People with a confirmed diagnosis of CD123-positive AML (a type of blood cancer) or BPDCN (a rare blood cancer), where the disease has come back or has not responded to previous treatments — specific criteria apply to each condition separately (confirm with trial site)
  • People expected to live for more than 12 weeks
  • People who are reasonably physically active and able to care for themselves, as measured by a standard medical scoring tool called the ECOG scale (scores 0–2)
  • People who do not have a severe mental health disorder
  • People whose major organs are functioning at an acceptable level, including adequate blood cell counts, heart function, kidney function, liver function, and blood oxygen levels (specific thresholds apply — confirm with trial site)
  • People, or their legal guardian, who are willing to sign a consent form confirming they understand and agree to take part in the trial

Who may not be able to join:

  • People who have cancer that has spread to the central nervous system (brain and spinal cord) at the time of screening
  • People who have received certain anti-cancer treatments, such as chemotherapy, targeted therapy, or experimental drugs, within 14 days or a specific time period before joining (unless their disease clearly progressed during that treatment)
  • People who have had a stroke or epileptic seizure within the 6 months before screening
  • People who have an active or uncontrolled infection requiring treatment within 1 week before screening
  • People with certain serious heart conditions, including severe heart failure, a heart attack or major heart surgery within 6 months, significant irregular heartbeats, unexplained fainting episodes, or a history of severe heart muscle disease
  • People who have an active autoimmune disease that requires long-term immune-suppressing medication
  • People who have another current cancer, with some exceptions for certain treated skin cancers and other specific cancers that have been fully treated (confirm with trial site)
  • People who have received a live vaccine within 4 weeks before screening
  • People who are pregnant or breastfeeding, or people — male or female — who plan to have children within 1 year after receiving the trial treatment
  • People the trial doctors consider unsuitable for the study for other medical reasons

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 23 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: +86 13986102084

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
Chongqing Precision Biotech Co., Ltd
Registry
ClinicalTrials.gov
Start date
13 November 2024
Est. completion
30 October 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability]; Objective response rate (ORR), including complete response (CR) and partial response (PR), after CAR-NK infusion; overall survival (OS) after CAR-NK infusion; Duration of response (DOR) after CAR-NK infusion; recurrence free survival (RFS) after CAR-NK infusion; event free survival (EFS) after CAR-NK cells infusion

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: 23 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