Phase 2 Lymphoma Trial, Recruiting NCT05579132 Sponsor: MSD R&D (China) Co., Ltd. Condition: Lymphoma
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Phase 2 Lymphoma Trial, Recruiting

NCT05579132
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:

  • Adults aged 18 or older, or children aged 2 to 17 years old
  • People diagnosed with a type of blood cancer called precursor B-cell acute lymphoblastic leukemia (B-ALL), with more than 5% cancer cells found in the bone marrow
  • People with B-ALL that does not involve a genetic change called the Philadelphia chromosome (Ph-negative), AND whose cancer meets at least one of these conditions: the cancer did not go into remission after the first round of treatment; the cancer did not go into remission after a second round of treatment; the cancer came back within 12 months of first going into remission; the cancer has relapsed a second time or more; or the cancer came back after a bone marrow/stem cell transplant from a donor
  • People with B-ALL that does involve the Philadelphia chromosome (Ph-positive), who have already received two or more targeted medicines called tyrosine kinase inhibitors (TKIs) and whose cancer meets the relapse or treatment-failure conditions listed above — or people with a specific genetic mutation called T315I (confirm with trial site)

Who may not be able to join:

  • People who have a history of a related blood cancer called Burkitt's leukemia
  • People who received a treatment targeting a protein called CD19 within the past 3 months
  • People who had a donor stem cell or bone marrow transplant within the past 12 weeks
  • People who previously received a type of cell therapy called CAR-T cell treatment within the past 3 months
  • People who have a significant history of, or current, brain or nervous system disease
  • People who have had cancer spread to the brain or the membranes surrounding the brain, or whose cancer in the brain is not currently controlled
  • People with a history of immune system deficiency, including anyone who has previously tested positive for HIV
  • People with a history of serious heart or blood vessel disease affecting the heart or brain
  • People who have an active autoimmune disease (where the immune system attacks the body) that may flare up

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 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: Jianxiang Wang, Dr., Institute of Hematology & Blood Diseases Hospital, China

Phone: 1-888-577-8839

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
MSD R&D (China) Co., Ltd.
Registry
ClinicalTrials.gov
Start date
1 November 2022
Est. completion
30 June 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Dose Escalation Phase: Number of Participants who Experience at Least One Adverse Event (AE); Dose Escalation Phase: Number of Participants who Discontinue Study Treatment Due to an AE; Dose Escalation Phase: Number of Participants Who Experience a Dose-limiting Toxicity (DLT); Dose Escalation Phase: Maximum Tolerated Dose (MTD) of MK-1045; Phase II: Complete Remission (CR) Rate

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