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NCT06722183RECRUITINGanonymous

FUTURE Platform Trial - A Phase II Platform Trial of Futibatinib in Combination With (Chemo)Immunotherapy in Colorectal Cancer and Other Solid Tumor Entities

Sponsor

Source record

Institut für Klinische Krebsforschung IKF GmbH at Krankenhaus Nordwest

Phase

Source record

PHASE2

Modality

AI-normalized

monoclonal antibody

Target

AI-normalized

Futibatinib orally administered, Tislelizumab (i.v. 200mg)

Indication / condition

AI-normalized

Colorectal Cancer

Intervention

Source record

Futibatinib orally administered, Tislelizumab (i.v. 200mg)

Source & freshness

Source record

NCT ID

NCT06722183

Original source

ClinicalTrials.gov

Source last updated

Dec 24, 2025

Ingested at

May 23, 2026

Internal sync

Jun 05, 2026

Model version

trialsignal-ai-v1

Normalized confidence

88%

Validation status

validated

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View original source fields

NCT ID

NCT06722183

Title

FUTURE Platform Trial - A Phase II Platform Trial of Futibatinib in Combination With (Chemo)Immunotherapy in Colorectal Cancer and Other Solid Tumor Entities

Sponsor

Institut für Klinische Krebsforschung IKF GmbH at Krankenhaus Nordwest

Status

RECRUITING

Phase

PHASE2

Condition raw

Colorectal Cancer

Condition normalized

Colorectal Cancer

Modality raw

colorectal cancer

Modality normalized

monoclonal antibody

Target raw

Futibatinib orally administered, Tislelizumab (i.v. 200mg)

Target normalized

Futibatinib orally administered, Tislelizumab (i.v. 200mg)

Interventions

Futibatinib orally administered, Tislelizumab (i.v. 200mg)

Public preview

Source record

FUTURE Platform Trial - A Phase II Platform Trial of Futibatinib in Combination With (Chemo)Immunotherapy in Colorectal Cancer and Other Solid Tumor Entities is a PHASE2 clinical asset sponsored by Institut für Klinische Krebsforschung IKF GmbH at Krankenhaus Nordwest in Colorectal Cancer. SEO and diligence focus: Futibatinib orally administered, Tislelizumab (i.v. 200mg), endpoint relevance, enrollment feasibility, competitive positioning, readout timing and IP durability.

AI-generated analysis supports research triage only. Verify source records, publications, sponsor disclosures and IP databases before making diligence decisions. Model: trialsignal-ai-v1.

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