Clinical Trials

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SCCA Clinical Studies: Phase I Program

 

RO5429083 Metastatic and/or Locally Advanced, CD44-Expressing, Malignant Solid Tumors
Open-Label Multicenter 2-Arm Phase I Study of RO5429083 With Dose-Escalation and Extension Cohorts, and Imaging Cohorts With RO5429083 and 89Zr-labeled RO5429083, in Patients With Metastatic and/or Locally Advanced, CD44-Expressing, Malignant Solid Tumors

Investigator: Andrew L. Coveler, MD;   Conditions: Neoplasms;    Status: Recruiting;   Study ID: NCT01358903

MDX-1105 for Advanced or Recurrent Cancer (UW08038)
A Phase 1, Open-label, Dose-escalation, Multidose Study of MDX-1105 Administered Every 14 Days in Subjects With Selected Advanced or Recurrent Solid Tumors

Investigator: Scott S. Tykodi, MD, PhD;   Conditions: Renal Cell Carcinoma, Non-small Cell Lung Cancer, Malignant Melanoma, Epithelial Ovarian Cancer, Colorectal Adenocarcinoma;    Status: Recruiting;   Study ID: NCT00729664

TKI258 for Advanced Renal Cell Cancer (CTK1258A2107)
A Phase I/II Multi-center, Open Label Study of TKI258 Administered Orally on an Intermittent Schedule in Adult Patients With Advanced or Metastatic Renal Cell Cancer (RCC)

Investigator: Scott S. Tykodi, MD, PhD ;   Conditions: Advanced/ Metastatic Renal Cell Cancer;    Status: Closed;   Study ID: NCT00715182

PF-04449913 for Hematologic Malignancies (B1371001)
A Phase 1 Study To Evaluate The Safety, Pharmacokinetics, And Pharmacodynamics Of PF 04449913, An Oral Hedgehog Inhibitor, Administered As Single Agent In Select Hematologic Malignancies

Investigator: Vivian Oehler, M.D,;   Conditions: Hematologic Malignancies;    Status: Recruiting;   Study ID: NCT00953758

SGN-35 for Lymphoma (UW 09043)
An Open-Label Clinical Pharmacology Study of Brentuximab Vedotin (SGN-35) in Patients With CD30-Positive Hematologic Malignancies: CYP3A4 Drug-Drug Interactions, Excretion, and Special Populations

Investigator: Dr. Ajay Gopal;   Conditions: Hodgkin's Lymphoma, , Large-Cell Anaplastic Lymphoma, Non-Hodgkin's Lymphoma;    Status: Recruiting;   Study ID: NCT01026415

PARP Inhibitor ABT-888 with Carboplatin & Gemcitabline (M10-758) (UW09039)
A Phase 1 Study of ABT-888 (Veliparib) in Combination With Carboplatin (Paraplatin) and Gemcitabline (Gemzar) in Subjects With Advanced Solid Tumors

Investigator: Heidi J. Gray, MD;   Conditions: Advanced Solid Tumors;    Status: Not Recruiting;   Study ID: NCT01063816

PARP Inhibitor ABT-888 with Cisplatin and Vinorelbine (7161)
Phase I Study of ABT-888 (Veliparib) in Combination With Cisplatin and Vinorelbine (Navelbine) for Patients With Advanced Triple Negative Breast Cancer and/or BRCA-Mutation Associated Breast Cancer

Investigator: Eve Rodler, MD;   Conditions: Advanced Breast Cancer;    Status: Recruiting;   Study ID: NCT01104259

Dose-Escalation Study of AGS-16M8F for Advanced Renal Cancer
A Phase 1, Open-label, Multi-center, Dose Escalation Study of the Safety and Pharmacokinetics of AGS-16M8F Monotherapy in Subjects With Advanced Renal Cell Carcinoma

Investigator: Dr John Thompson;   Conditions: Renal Cell Carcinoma;    Status: Recruiting;   Study ID: NCT01114230

MLN8237, an Aurora A Kinase Inhibitor w/ Weekly Paclitaxel (C14008).
Randomized Phase 2 Study of MLN8237, an Aurora A Kinase Inhibitor, Plus Weekly Paclitaxel or Weekly Paclitaxel Alone in Patients With Recurrent Epithelial Ovarian, Fallopian Tube, or Primary Peritoneal Cancer, Preceded by a Phase 1 Portion in Patients With Ovarian or Breast Cancer

Investigator: Barbara A. Goff, MD;   Conditions: Ovarian Carcinoma, Fallopian Tube Cancer, Peritoneal Cancer, Breast Carcinoma;    Status: Recruiting;   Study ID: NCT01091428

LDK378 for Tumors with ALK Mutation (UW10038)
A Dose Finding Study With Oral LDK378 in Patients With Tumors Characterized by Genetic Abnormalities in Anaplastic Lymphoma Kinase (ALK)

Investigator: Laura Chow, MD;   Conditions: Tumors Characterized by Genetic Abnormalities of ALK;    Status: Recruiting;   Study ID: NCT01283516

TRU-016 w/ Rituximab and Bendamustine for Lymphoma
A Phase 1b/2 Study of TRU-016 in Combination With Rituximab and Bendamustine in Subjects With Relapsed Indolent Lymphoma

Investigator: Ajay K. Gopal, MD;   Conditions: Relapsed Indolent B-cell Lymphoma;    Status: Recruiting;   Study ID: NCT01317901

PF-05082566 for Advanced Cancer or B-Cell Lymphoma
A Phase 1 Study Of PF-05082566 As A Single Agent In Patients With Advanced Cancer, And In Combination With Rituximab In Patients With Non-Hodgkin's Lymphoma (NHL)

Investigator: Ajay K. Gopal, MD;   Conditions: Non-Hodgkin's Lymphoma (NHL);    Status: Recruiting;   Study ID: NCT01307267

GA101 (RO5072759) for Previously Untreated Chronic Lymphocytic Leukemia (2514)
An Open-Label, Multicenter, Phase Ib Trial of GA101 (RO5072759) in Combination With Chemotherapy in Patients With Previously Untreated Chronic Lymphocytic Leukemia

Investigator: Ajay K. Gopal, MD;   Conditions: Chronic Lymphocytic Leukemia;    Status: Recruiting;   Study ID: NCT01300247

PARP Inhibitor BMN 673 for Advanced Hematological Malignancies
Phase 1, Two-arm, Open-label Study of Once Daily, Oral BMN 673 in Patients With Advanced Hematological Malignancies

Investigator: Ajay K. Gopal, MD;   Conditions: Acute Myeloid Leukemia, Myelodysplastic Syndrome, Chronic Lymphocytic Leukemia, Mantle Cell Lymphoma;    Status: Recruiting;   Study ID: NCT01399840

PEGPH20 for Stage IV Previously Untreated Pancreatic Cancer (2542.00)
A Phase 1b/2 Multicenter, International, Randomized, Double Blind, Placebo-Controlled, Study of Gemcitabine (Gemzar) Combined With PEGPH20 Compared to Gemcitabine Combined With Placebo in Patients With Stage IV Previously Untreated Pancreatic Cancer

Investigator: Sunil Hingorani, MD, PhD;   Conditions: Pancreatic Cancer;    Status: Recruiting;   Study ID: NCT01453153

Inotuzumab Ozogamicin for Acute Lymphocytic Leukemia
An Open-Label, Phase 1 Study Of Inotuzumab Ozogamicin In Subjects With Relapsed Or Refractory CD22-Positive Acute Lymphocytic Leukemia

Investigator: Stephen H. Petersdorf, MD;   Conditions: Acute Lymphocytic Leukemia;    Status: Recruiting;   Study ID: NCT01363297

IL-21/Ipilimumab Combination for Melanoma
A Phase I Dose Escalation Study of BMS-982470 (Recombinant Interleukin 21, rIL-21) in Combination With Ipilimumab in Subjects With Unresectable Stage III or Stage IV Melanoma

Investigator: Shailender Bhatia, M.D.;   Conditions: Melanoma;    Status: Recruiting;   Study ID: NCT01489059