XL647: Clinical Trials

13 trials of XL647, newest first

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9 completed, 3 terminated, 1 withdrawn. 8 Phase 2, 6 Phase 1, 1 Phase 3.

By phase and status

PhaseTrialsStatus
Phase 28Completed 6, Terminated 2
Phase 16Completed 4, Terminated 1, Withdrawn 1
Phase 31Terminated 1

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Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.

TrialPhaseStatusSponsorEnrollmentStartUpdated
Study of the Efficacy and Safety of Tesevatinib in Subjects With ADPKD
Tesevatinib, Placebo - Autosomal Dominant Polycystic Kidney, ADPKD
Phase 2CompletedKadmon, a Sanofi Company802017-10-122023-02-06
A Safety, Pharmacokinetic, Single Ascending Dose Study of Tesevatinib in Pediatric Subjects With Autosomal Recessive Polycystic Kidney Disease (ARPKD)
Tesevatinib - Polycystic Kidney, Autosomal Recessive
Phase 1CompletedKadmon Corporation, LLC102017-08-242022-05-11
Study of Tesevatinib Monotherapy in Patients With Recurrent Glioblastoma
Tesevatinib - Glioblastoma, Recurrent Glioblastoma
Phase 2CompletedKadmon Corporation, LLC402016-06-012021-09-22
Long-Term Treatment and Follow up of Subjects Completing 24 Months of Treatment With Tesevatinib on Study KD019-101
tesevatinib - Autosomal Dominant Polycystic Kidney Disease (ADPKD)
Phase 2TerminatedKadmon Corporation, LLC152015-12-252022-05-25
Phase 2 Study of Study of Tesevatinib in Subjects With NSCLC and Brain or Leptomeningeal Metastases
Tesevatinib - Non-Small Cell Lung Cancer, Leptomeningeal Metastases
Phase 2CompletedKadmon Corporation, LLC362015-11-012022-03-16
Study of the Combination of KD019 and Trastuzumab in Subjects With HER2-Positive Metastatic Breast Cancer
Tesevatinib, Trastuzumab - HER-2 Positive Breast Cancer, Metastatic Malignant Neoplasm to Brain
Phase 1 / Phase 2TerminatedKadmon Corporation, LLC172014-05-012022-04-27
A Safety, Pharmacokinetic & Dose-Escalation Study of KD019 in Subjects With Autosomal Dominant Polycystic Kidney Disease
Tesevatinib - Polycystic Kidney, Autosomal Dominant
Phase 1 / Phase 2CompletedKadmon, a Sanofi Company692012-10-112022-11-08
KD019 Versus Erlotinib in Subjects With Stage IIIB/IV Non Small Cell Lung Cancer With Progression After First- or Second-Line Chemotherapy
KD019, Erlotinib - Carcinoma, Non-Small-Cell Lung
Phase 3TerminatedKadmon Corporation, LLC82011-12-142022-05-13
Safety Study of XL647 and XL147 Administered in Combination Daily in Adults With Solid Tumors
XL647, XL147 - Cancer, Non-small-cell Lung Cancer
Phase 1WithdrawnExelixis2008-06-012015-08-20
Study of XL647 in Subjects With NSCLC Who Have Progressed After Responding to Treatment With Gefitinib or Erlotinib
XL647 - Carcinoma, Non-Small-Cell Lung
Phase 2CompletedKadmon Corporation, LLC412007-05-012022-05-13
Study of XL647 Administered Orally Daily to Patients With Solid Tumors
XL647 - Cancer
Phase 1CompletedKadmon Corporation, LLC312006-07-012022-05-13
Study of XL647 in Subjects With Non-Small-Cell Lung Cancer
XL647 - Non-small-cell Lung Cancer
Phase 2CompletedKadmon Corporation, LLC552006-07-012022-05-13
Safety and Pharmacokinetics of XL647 Administered Orally to Subjects With Solid Tumors
XL647 - Cancer
Phase 1CompletedKadmon Corporation, LLC412004-06-012022-05-13

Conditions studied

Carcinoma, Non-Small-Cell Lung (5)  ·  Brain Neoplasms (3)  ·  Neoplasms (3)  ·  Polycystic Kidney, Autosomal Dominant (3)  ·  Polycystic Kidney Diseases (2)  ·  Breast Neoplasms (1)  ·  Glioblastoma (1)  ·  Meningeal Carcinomatosis (1)  ·  Polycystic Kidney, Autosomal Recessive (1)

Sponsors

Kadmon Corporation, LLC (10)  ·  Kadmon, a Sanofi Company (2)  ·  Exelixis (1)

Countries

United States (13)

Top investigators

Harold Keer, M.D., Ph.D. (1)

Results publications

PMID 41385299