Phase 1 Lymphoma Trial, Recruiting NCT05341557 Sponsor: Betta Pharmaceuticals Co., Ltd. Condition: Lymphoma
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Phase 1 Lymphoma Trial, Recruiting

NCT05341557
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:

  • People aged 18 to 65 (in the dose escalation phase) or aged 18 and over (in the dose expansion phase), of any gender
  • People whose general health and ability to carry out daily activities meets a standard scoring level known as ECOG performance status 0 or 1 (confirm with trial site)
  • In the dose escalation phase: people with a confirmed advanced or metastatic solid tumour (not liver cancer) or relapsed/returning lymphoma, whose cancer has continued to grow after standard treatments, who could not tolerate standard treatments, who have declined standard treatments, or for whom no standard treatments exist
  • In the dose expansion phase: people with confirmed advanced or metastatic non-small cell lung cancer without certain gene mutations, relapsed or returning lymphoma, liver cancer (hepatocellular carcinoma) with a specific liver function score, or other solid tumours where standard treatment has failed, is not tolerated, is declined, or does not exist
  • People who have at least one measurable or evaluable area of cancer that can be tracked on scans, assessed using standard measurement methods appropriate to their cancer type
  • People whose organs (such as liver, kidneys, and blood system) are functioning at an adequate level

Who may not be able to join:

  • In the dose escalation phase: people who have previously received certain immunotherapy drugs that target PD-1, PD-L1, or PD-L2
  • In the dose expansion phase: people who have received PD-1, PD-L1, or PD-L2 immunotherapy within the 28 days before treatment starts, or people who have previously experienced a severe (Grade 3 or higher) immune-related side effect from immunotherapy
  • People who have previously received certain other treatments that target specific immune cells called T cells (confirm specific agents with trial site)
  • People who have been taking steroid medicines at a dose of 10 mg per day or more (or equivalent) in the two weeks before starting the trial
  • People who have not waited long enough since finishing previous cancer treatments, certain other medications, or vaccines, as specified by the trial protocol (confirm timeframes with trial site)
  • People who have had major surgery within the past four weeks, or who have serious unstable health conditions, active or symptomatic cancer spread to the brain, another active cancer, autoimmune disease, certain lung conditions, significant heart disease, active bleeding or clotting problems, active serious infections, difficulty swallowing or absorbing medicines, or a history of chronic diarrhoea
  • People who are pregnant or breastfeeding
  • People whom the trial investigators consider unsuitable to participate 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 20 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

Principal Investigator: Yuankai Shi, Ph.D, Cancer Institute and Hospital, Chinese Academy of Medical Sciences

Phone: 010-67781331

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
Betta Pharmaceuticals Co., Ltd.
Registry
ClinicalTrials.gov
Start date
29 August 2022
Est. completion
1 December 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

The adverse events (AEs); Determine the recommended Phase II dose (RP2D)

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: 20 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