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NCT05155709CompletedPhase 1

A Study of Siremadlin in Combination With Venetoclax Plus Azacitidine in Adult Participants With Acute Myeloid Leukemia (AML) Who Are Ineligible for Chemotherapy.

A Phase Ib/II Open Label Dose Confirmation, Proof of Concept Study of Siremadlin in Combination With Venetoclax Plus Azacitidine in Unfit Adult AML Participants Who Responded Sub-optimally to First-line Venetoclax Plus Azacitidine Treatment and in Participants With Newly Diagnosed Unfit AML Presenting With High-risk Clinical Features

Source: ClinicalTrials.gov · Last updated 7 May 2026

Brief summary (registry, in English)

A study of siremadlin in combination with venetoclax plus azacitidine in adult participants with AML who are ineligible for chemotherapy. The primary purpose of this study was to assess whether siremadlin in combination with venetoclax plus azacitidine can enhance the clinical response in unfit AML participants without unacceptable levels of treatment-emergent toxicities.

Status (registry)
Completed
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
14 (actual)
First submitted
20 Oct 2021
Start date
17 May 2022
Primary completion date
17 Apr 2024
Lead sponsor
Novartis Pharmaceuticals
NCT number
NCT05155709
EudraCT number
2021-001165-21

What you commit to

  • Study type: Interventional · Phase 1
  • Participants enrolled: 14
  • From 17 May 2022 to the primary completion date, 17 Apr 2024
  • 10 sites in 7 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior exposure to MDM2-inhibitor therapy at any time.
  • Participants treated with FLT3 inhibitors for AML indication are not eligible.
  • Participants who require treatment with moderate or strong CYP3A4 inducers within 14 days prior to starting study treatment, or are expected to receive moderate or strong CYP3A4 inducers during the entire study
  • Participants who require treatment with substrates of CYP3A4/5 with a narrow therapeutic index.

Other illness

  • Participants with AML-M3 / APL (Acute promyelocytic leukemia) with PML-RARA (Promyelocytic leukemia/retinoic acid receptor alpha) or with AML secondary to Down's syndrome.

Other

  • Participants with TP53 mutation positive.
  • Participants with del17p.

Who the study is looking for

  • Age at the date of signing the informed consent form (ICF):
    • Arm 1 and Arm 2: ≥ 18 years
  • Participants diagnosed with AML based on WHO 2016 classification (Arber et al 2016) who are ineligible for standard induction chemotherapy and:
    • Arm 1 : have received at least 2 cycles and not more than 4 cycles of first-line venetoclax plus azacitidine treatment and have not achieved a CR, CRi, CRh or MLFS.
    • Arm 2 : newly diagnosed AML with adverse genetic risk stratification (according to ELN 2022) (except TP53 mutation positive participants).
  • Participant (in both arms) must be considered ineligible for standard of care intensive induction chemotherapy defined by the following:
    • 75 years of age; OR
    • 18 to 74 years of age with at least one of the following co-morbidities: Eastern Cooperative Oncology Group (ECOG) Performance Status of 2 or 3; Cardiac history of congestive heart failure (CHF) requiring treatment or Ejection Fraction ≤ 50% or chronic stable angina; DLCO ≤ 65% or FEV1 ≤ 65%.
  • Participants must have an ECOG performance status:
    • 0 to 2 for participants ≥ 75 years of age. OR 0 to 3 for participants ≥ 18 to 74 years of age.
  • WBC \< 25x109/L
  • AST and ALT ≤ 3 × ULN
  • Estimated Glomerular Filtration Rate (eGFR)≥ 60 mL/min/1.73 m2

Age in the registry: 18 years to 99 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (10)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Novartis Investigative Site
Coordinator of this site? Confirm its status
Hong KongHong Kong SAR ChinaUnknown status
Novartis Investigative Site
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BudapestHungaryUnknown status
Novartis Investigative Site
Coordinator of this site? Confirm its status
BeershebaIsraelUnknown status
Novartis Investigative Site
Coordinator of this site? Confirm its status
JerusalemIsraelUnknown status
Novartis Investigative Site
Coordinator of this site? Confirm its status
BolognaItalyUnknown status
Novartis Investigative Site
Coordinator of this site? Confirm its status
Alor StarMalaysiaUnknown status
Novartis Investigative Site
Coordinator of this site? Confirm its status
Kuala SelangorMalaysiaUnknown status
Texas Oncology Sammons Cancer Center
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DallasUnited StatesUnknown status
Oregon Health Sciences University
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PortlandUnited StatesUnknown status
Novartis Investigative Site
Coordinator of this site? Confirm its status
IzmirTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.