OncoMatch/Clinical Trials/NCT05186012
APG-1252 Monotherapy or in Combination With Other Therapeutic Agent in Subjects With Relapsed or Refractory Non-Hodgkin Lymphoma
Is NCT05186012 recruiting? Yes, currently enrolling (May 2026). This Phase 1/2 trial studies multiple treatments including APG-1252 and Chidamide for nhl, adult.
Treatment: APG-1252 · Chidamide — The purpose of this study is to assess the safety, pharmacokinetic, pharmacodynamic and efficacy of APG-1252 single agent and in combination with other therapeutic agent in patients with NHL.
Check if I qualifyExtracted eligibility criteria
Cancer type
Non-Hodgkin Lymphoma
Performance status
ECOG 0–1(Restricted strenuous activity)
Prior therapy
Must have received:
previously treated with at least 1 prior line of therapy
Cannot have received: allogeneic cell transplant
Prior history of allogeneic cell transplant
Cannot have received: adoptive cellular immunotherapy
Exception: allowed if >2 years prior
adoptive cellular immunotherapy within 2 years
Cannot have received: autologous hematopoietic stem cell transplantation
Exception: allowed if >6 months prior
autologous hematopoietic stem cell transplantation within 6 months
Cannot have received: monoclonal antibody therapy
Exception: allowed if >4 weeks prior
Monoclonal antibody therapy within 4 weeks prior to the first dose
Cannot have received: anti-cancer therapy
Exception: allowed if >14 days prior
Received anti-cancer therapy within 14 days prior to the first dose of therapy, including chemotherapy, radiotherapy, immunotherapy or hormone therapy for anti-tumor purposes
Cannot have received: investigational agent
Exception: allowed if >28 days prior
28 days for any investigational agent prior to the first dose of therapy
Cannot have received: BCL-xL inhibitor
Prior exposure to BCL-xL inhibitor
Lab requirements
Blood counts
Adequate bone marrow function
Kidney function
Adequate renal function
Liver function
Adequate hepatic function
Cardiac function
Corrected QT interval (QTcB or QTcF ) ≤ 450ms (male), or ≤ 470ms (female)
Adequate bone marrow function. Adequate hepatic, renal and coagulation function. Corrected QT interval (QTcB or QTcF ) ≤ 450ms (male), or ≤ 470ms (female).
Structured fields extracted by AI. May contain errors — verify against the official protocol.
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