Clinical Trials Directory

Trials / Sponsors / Synta Pharmaceuticals Corp.

Synta Pharmaceuticals Corp.

Industry · 25 registered clinical trials.

StatusTrialPhaseStarted
TerminatedA Phase 3 Study of Ganetespib in Combination With Docetaxel Versus Docetaxel Alone in Patients With Advanced N
Non-Small-Cell Lung Adenocarcinoma, Non-small Cell Lung Cancer Stage IIIB, Non-small Cell Lung Cancer Stage IV
Phase 32013-04-01
CompletedAn Open-Label Multicenter Phase 2 Window of Opportunity Study Evaluating Ganetespib in Women With Breast Cance
Breast Cancer, HER-2 Positive Breast Cancer, Triple Negative Breast Cancer
Phase 22012-07-01
CompletedA Study of Ganetespib in Subjects With ALK-Positive Non-Small-Cell Lung Cancer (NSCLC)
Non Small Cell Lung Cancer
Phase 22012-04-01
TerminatedStudy of Ganetespib (STA-9090) + Docetaxel in Advanced Non Small Cell Lung Cancer
Non-small Cell Lung Cancer Stage IIIB, Non-small Cell Lung Cancer Stage IV, Non-small Cell Lung Cancer Metastatic
Phase 2 / Phase 32011-05-01
UnknownStudy Elesclomol Sodium in Patients With Relapsed or Refractory Acute Myeloid Leukemia
Acute Myeloid Leukemia
Phase 12011-01-01
CompletedA Dose Escalation Study of STA-9090 and Docetaxel in Patients With Solid Tumors
Solid Tumor Malignancies
Phase 12010-07-01
CompletedA Study Evaluating STA-9090 in Patients With Metastatic and/or Unresectable Gastrointestinal Stromal Tumor (GI
Gastrointestinal Stromal Tumor
Phase 22010-01-01
CompletedA Study of the HSP90 Inhibitor, STA-9090 in Subjects With Stage IIIB or IV Non-Small Cell Lung Cancer (NSCLC)
Non Small Cell Lung Cancer
Phase 22009-11-01
CompletedA Phase 1 Study of the HSP90 Inhibitor, STA-9090 in Subjects With Acute Myeloid Leukemia, Acute Lymphoblastic
Acute Myeloid Leukemia, Acute Lymphoblastic Leukemia, Blast-phase Chronic Myelogenous Leukemia
Phase 12009-08-01
CompletedSTA-9090 for Treatment of AML, CML, MDS and Myeloproliferative Disorders
AML, CML, MDS
Phase 12009-03-01
SuspendedA Safety Study to Determine the Maximum Tolerated Dose of Elesclomol Sodium in Patients With Solid Tumors
Metastatic Solid Tumors
Phase 12009-01-01
CompletedA Study to Determine the Maximum Tolerated Dose of Elesclomol Sodium Given With a Fixed Dose of Docetaxel and
Prostate Cancer
Phase 12008-11-01
CompletedStudy of STA-9090, Administered Once-Weekly in Patients With Solid Tumors
Solid Tumors
Phase 12007-10-01
UnknownStudy of STA-9090, Administered Twice-Weekly in Patients With Solid Tumors
Solid Tumors
Phase 12007-10-01
TerminatedElesclomol (STA-4783) With Paclitaxel Versus Paclitaxel Alone in Melanoma
Melanoma
Phase 32007-08-01
CompletedA Randomized, Double-blind, Placebo-controlled Clinical Study of the Oral IL-12/23 Inhibitor, STA-5326 Mesylat
Active, Moderate to Severe Rheumatoid Arthritis
Phase 22005-12-01
CompletedStudy of STA-5326 Mesylate in Patients With Moderate to Severe Crohn's Disease
Crohn's Disease
Phase 22005-11-01
CompletedStudy of STA-5326 Mesylate in Patients With Moderate to Severe Crohn's Disease
Crohn's Disease
Phase 22005-08-01
CompletedA Study of STA-4783 in Combination With Weekly Paclitaxel for Treatment of Patients With Soft Tissue Sarcomas
Soft Tissue Sarcoma
Phase 22004-07-01
CompletedA Phase I Study of STA-5312 in Subjects With Advanced or Metastatic Solid Tumors
Advanced or Metastatic Solid Tumors
Phase 12004-06-01
CompletedSTA-4783/Paclitaxel or Paclitaxel Alone in Melanoma
Melanoma
Phase 1 / Phase 22004-05-01
CompletedSTA-4783 in Combination With Paclitaxel and Carboplatin for the Treatment of Chemotherapy Naive Patients With
Stage IIIB Non-Small Cell Lung Cancer, Stage IV Non-Small Cell Lung Cancer
Phase 1 / Phase 22004-03-01
CompletedSTA-5312 Administered on Alternate Weekdays Every Two Weeks to Patients With Hematologic Malignancies and Pati
Hematological Malignancies, Leukemia, Lymphoma
Phase 12004-02-01
CompletedSTA-5326 in Crohn's Disease Patients
Crohn's Disease
Phase 1 / Phase 22004-02-01
CompletedSTA-4783 and Paclitaxel for Treatment of Solid Tumors
Neoplasms
Phase 12003-01-01