Study of Inlexisertib (DCC-3116) in Participants With RAS/MAPK Pathway Mutant Solid Tumors

Stopped early · Phase 1

Conditions studied: Non-Small Cell Lung Cancer, Advanced Solid Tumor, Metastatic Solid Tumor

In brief

This is a multicenter, open label, first in human (FIH) study of inlexisertib as monotherapy, and in combination with trametinib, binimetinib, or sotorasib in participants with advanced or metastatic solid tumors with RAS/MAPK pathway mutation. The study consists of 2 parts, a dose-escalation phase, and an expansion phase.

Key facts

Study ID: NCT04892017
Run by: Deciphera Pharmaceuticals, LLC
People needed: 91
Starts: 2021-06-15
Expected to finish: 2026-03-30
Last updated by the study team: 2026-04-08

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Male or female participants ≥18 years of age
Dose Escalation Phase (Part 1):
Escalation Cohort B combination with trametinib and Cohort C combination with binimetinib closed on January 8, 2024.
Participants must have a pathologically confirmed diagnosis of an advanced or metastatic solid tumor with a documented RAS, NF1, or RAF mutations. A molecular pathology report documenting mutational status of RAS, NF1, or RAF must be available.
Progressed despite standard therapies, and received at least 1 prior line of anticancer therapy.
Participants with a documented mutation in BRAF V600E or V600K must have received approved treatments known to provide clinical benefit prior to study entry.
Participants enrolled in the inlexisertib and sotorasib cohort (Cohort D) must have a KRAS G12C mutation.
Dose Expansion Phase (Part 2):
Expansion Cohorts 1, 2, 3 and 4 combinations will not open for enrollment.
Cohort 5: Participants with KRAS G12C mutant NSCLC
Pathologically confirmed NSCLC with a documented mutation in KRAS G12C.
Received at least 1 prior line of systemic therapy in the advanced or metastatic setting.
Have not received prior sotorasib or other KRAS G12C inhibitor therapy.
Must provide a fresh tumor biopsy from a primary or metastatic cancer lesion if it can be biopsied with acceptable risk as determined by the Investigator.
Must have at least 1 measurable lesion according to Response Evaluation Criteria in Solid Tumors (RECIST), v1.1
Eastern Cooperative Oncology Group (ECOG) score of 0 to 2 (Dose Escalation) or 0 to 1 (Dose Expansion) at Screening
Adequate organ function and bone marrow function.
If a female of childbearing potential must have a negative pregnancy test prior to enrollment and agree to follow the contraception requirements.
Male participants must agree to follow contraception requirements.
Must provide signed consent to participate in the study and is willing to comply with study-specific procedures.

You may not qualify if…

Must not have received the following within the specified time periods prior to the first dose of study drug:
Prior therapies (anticancer or therapies given for other reasons) that are known strong or moderate inhibitors or inducers of CYP3A4 or P-glycoprotein (P-gp) including certain herbal medications (e.g., St. John's Wort): 14 days or 5× the half-life of the medication (whichever is longer)
All other prior anticancer therapies or any therapy that is investigational for the participant's condition with a known safety and PK profile: 14 days or 5× the half-life of the medication (whichever is shorter)
Investigational therapies with unknown safety and PK profile: 28 days. If there is enough data on the investigational therapy to assess the risk for drug-drug interactions and late toxicities of prior therapy as low, the Sponsor's Medical Monitor may approve a shorter washout of 14 days
Grapefruit or grapefruit juice: 14 days
Has a prior or concurrent malignancy that requires treatment or is expected to require treatment for active cancer during this study . Hormonal maintenance after treatment is allowed.
Have not recovered from all toxicities from prior therapy according to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE).
Presence or history of central nervous system (CNS) metastases or leptomeningeal disease, with some exceptions
New York Heart Association Class III or IV heart disease, active ischemia, or any other uncontrolled cardiac condition such as angina pectoris, clinically significant cardiac arrhythmia requiring therapy, uncontrolled hypertension, congestive heart failure, or myocardial infarction within 6 months prior to the first dose of study drug.
Prolongation of the QT interval corrected by Fridericia's formula (QTcF) based on repeated demonstration of QTcF >450 ms in males or >470 ms in females at screening, or history of long QT syndrome.
Left ventricular ejection fraction (LVEF) <50% at Screening
Systemic arterial thrombotic or embolic events within 6 months prior to the first dose of study drug
Systemic venous thrombotic events within 1 month prior to the first dose of study drug
Malabsorption syndrome
Major surgery within 4 weeks of the first dose of study drug. All surgical wounds must be healed and free of infection or dehiscence before the first dose of the study drug.
Any other clinically significant comorbidities.
For participants receiving inlexisertib and trametinib combination or inlexisertib and binimetinib combination: previous treatment with trametinib or binimetinib that resulted in treatment discontinuation due to intolerability as a result of an adverse event (AE) that was considered related to trametinib or binimetinib.
For participants receiving inlexisertib and sotorasib combination in Dose Escalation Part 1: previous treatment with sotorasib that resulted in treatment discontinuation due to intolerability as a result of an adverse event (AE) that was considered related to sotorasib.
For participants receiving inlexisertib and sotorasib combination: Use of proton pump inhibitors (PPIs) and H2 receptor antagonists that cannot be discontinued 3 days prior to the start of study drug administration.
Known allergy or hypersensitivity to any component of the investigational drug products.
Known human immunodeficiency virus unless the following requirements are met:
CD4 count >350/µL
No AIDS-defining opportunistic infection in the last 12 months
Stable anti-retroviral regimen with medications that are not prohibited by the protocol for at least 4 weeks with HIV viral load less than 400 copies/mL prior to enrollment.
Known active hepatitis B, active hepatitis C infection or if the participant is taking medications that are prohibited per protocol.

Where it is running

Massachusetts General Hospital — Boston, Massachusetts, United States
Washington University Siteman Cancer Center — St Louis, Missouri, United States
Rutgers Cancer Institute — New Brunswick, New Jersey, United States
Laura & Isaac Perlmutter Cancer Center at NYU Langone Health — New York, New York, United States
Oregon Health and Science University — Portland, Oregon, United States
Hospital of the University of Pennsylvania — Philadelphia, Pennsylvania, United States
NEXT Oncology — Austin, Texas, United States
The University of Texas MD Anderson Cancer Center — Houston, Texas, United States
NEXT Oncology — San Antonio, Texas, United States
University of Wisconsin Clinical Science Center — Madison, Wisconsin, United States

Full record on ClinicalTrials.gov

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