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Terminated Phase 1 Interventional

Study of DCC-3084 in Participants With Advanced Malignancies Driven by the Mitogen-Activated Protein Kinase (MAPK) Pathway

ClinicalTrials.gov ID: NCT06287463

Public ClinicalTrials.gov record NCT06287463. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 11:21 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Master Protocol for the Multi-Cohort, Open-Label, Phase 1/2 Study of DCC-3084 as Monotherapy and in Combination With Other Antitumor Agents in Participants With Advanced Malignancies Driven by the MAPK Pathway

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a multicenter clinical trial to evaluate DCC-3084 alone or in combination with other cancer therapies in participants with advanced cancers. Module A will enroll participants with advanced/metastatic solid tumors. Additional modules exploring other cancers may be added to the master protocol at a later date. Each module will be conducted in 2 parts: Part 1 (Dose Escalation) and Part 2 (Dose Expansion).

Study identification

NCT ID
NCT06287463
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1
Lead sponsor
Deciphera Pharmaceuticals, LLC
Industry
Enrollment
29 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 14, 2024 (Actual)
Primary completion
Feb 13, 2026 (Actual)
Completion
Feb 13, 2026 (Actual)
Last update posted
Mar 5, 2026

2024 – 2026

United States locations

U.S. sites
9
U.S. states
8
U.S. cities
9
Facility City State ZIP Site status
University of Southern California - Norris Comprehensive Cancer Center Los Angeles California 90033 —
University of California San Francisco (UCSF) Helen Diller Family Comprehensive Cancer Center San Francisco California 94158 —
SCRI HealthONE Denver Colorado 80218 —
SCRI Florida Cancer Specialists Orlando Florida 32827 —
Dana-Farber Cancer Institute Boston Massachusetts 02215 —
Roswell Park Comprehensive Cancer Center Buffalo New York 14263 —
SCRI Oncology Partners Nashville Tennessee 37203 —
NEXT Oncology San Antonio Texas 78229 —
NEXT Oncology Virginia Fairfax Virginia 22031 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06287463, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 5, 2026 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06287463 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →