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Find A Clinical Trial

Disease Type: Solid Tumors All

Trial ID 1336-0011
Sponsor ID

An open label phase Ib dose finding study of BI 836880 in combination with BI 754091 to characterize safety, tolerability, pharmacokinetics, pharmacodynamics and efficacy in patients with locally advanced or metastatic non-squamous Non-Small Cell Lung Cancer and in other solid tumors

Trial ID 20344
Sponsor ID SGNTUC-019

A Phase 2 Basket Study of Tucatinib in Combination with Trastuzumab in Subjects with Previously Treated, Locally-Advanced Unresectable or Metastatic Solid Tumors Driven by HER2 Alterations

Trial ID 20186
Sponsor ID BO41932


Trial ID 20286
Sponsor ID SGN00-002

Screening protocol to detect HER2 alterations required for enrollment on clinical research protocols of tucatinib (SGN00-002)

Principal Investigator
Keeran R. Sampat, MD
5 Locations
Trial ID ALK4230-A101
Sponsor ID Alkermes

A Phase 1/2 Study of ALKS 4230 Administered Intravenously as Monotherapy and in Combination with Pembrolizumab in Subjects with Advanced Solid Tumors- ARTISTRY-1

Trial ID RTX-240-01
Sponsor ID Rubius Therapeutics

PHASE 1/2 STUDY OF RTX-240 MONOTHERAPY Open label, multicenter, multidose, first-in-human Phase 1/2 study of RTX-240 for the treatment of patients with relapsed/refractory or locally advanced solid tumors.

Trial ID BBI-20201001
Sponsor ID Bolt Biotherapeutics, Inc.

Phase 1 Study of BDC-1001 as a Single Agent and in Combination with Pembrolizumab in Patients with Advanced and HER2 Expressing Solid Tumors.

Trial ID 19079
Sponsor ID Incyte

(INCB 54828-207) A Phase 2, Open-Label, Single-Arm, Multicenter Study to Evaluate the Efficacy and Safety of Pemigatinib in Participants With Previously Treated Locally Advanced/Metastatic or Surgically Unresectable Solid Tumor Malignancies Harboring Activating FGFR Mutations or Translocations (FIGHT-207)

Principal Investigator
Timothy A. McCarthy, MD
Trial ID 18027
Sponsor ID

A Phase 1a / 1b, First-in-human, Open-label, Dose-escalation, Safety, Pharmacokinetic, and Pharmacodynamic Study of Oral TP-0903 Administered Daily for 21 Days to Patients with Advanced Solid Tumors (TP-0903-101)