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Clinical Trial Listings: Neoplasms

Product Name/CompoundUnique Protocol IDConditions Brief TitleStudy PhaseStatus
MAC-321 3128K1-201 Carcinoma, Non-Small-Cell Lung, Lung Neoplasms, Study evaluating MAC-321 in Non-small Cell Lung Cancer Refractory to Platinum-based Therapy Phase 2 No longer recruiting
EKB-569 3095A1-201 Non-Small-Cell Lung Carcinoma, Carcinoma, Non-Small Cell Lung, Lung Neoplasms, Study evaluating EKB-569 in Advanced Non-Small Cell Lung Cancer Phase 2 No longer recruiting
MST-997 3161K1-100 Neoplasms, Study evaluating MST-997 in Advanced Malignant Solid Tumors Phase 1 Terminated
HKI-272 3144A1-200 Carcinoma, Non-Small-Cell Lung, Lung Neoplasms, Study Evaluating the Safety of HKI-272 in Subjects with Advanced Non-Small Cell Lung Cancer Phase 2 Completed
TTI-237 3162K1-100 Tumors, Neoplasms, Study Evaluating TTI-237 in Advanced Malignant Solid Tumors. Phase 1 Terminated
Piperacillin/Tazobactam (Tazocin) 0910B1-308 Hematologic Neoplasms, Study Comparing the Safety and Efficacy of Piperacillin/Tazobactam to Cefepime in Patients with Hematologic Malignancy or Lymphoma Phase 3 Completed
CMD-193 3152K1-101 Neoplasms, Study Evaluating Intravenous CMD-193 in Subjects with Advanced Malignant Solid Tumors Phase 1 Terminated
temsirolimus 3066K1-139 Adenocarcinoma, Neoplasms, Study evaluating biomarkers in Relapsed/Refractory Pediatric Solid Tumors Phase 1/Phase 2 Recruiting
SKI-606 3160A1-100 Neoplasms, Study Evaluating SKI-606 in Advanced Malignant Solid Tumors Phase 1 Active, not recruiting
HKI-272 3144A1-201 Breast Neoplasms, Neoplasms, Study Evaluating HKI-272 in Subjects with Advanced Breast Cancer Phase 2 Active, not recruiting
Interferon Alfa 3066K1-304 Carcinoma, Renal Cell, Kidney Neoplasms, Study Evaluating Interferon and CCI-779 in Advanced Renal Cell Carcinoma Phase 3 Active, not recruiting
MAC-321 3128K1-200 Colorectal Neoplasms, Colonic Neoplasms, Rectal Neoplasms, Study evaluating MAC-321 in Colorectal Cancer Phase 2 No longer recruiting
HKI-272 3144A1-102 Breast Neoplasms, Study evaluating HKI-272 in tumors Phase 1 Completed
piperacillin-tazobactam 100943 hematological malignancy, leukemia, myelodysplasia, lymphoma, myeloma, stem cell transplantation, Study Comparing piperacillin-tazobactam versus piperacillin-tazobactam plus glycopeptide in neutropenic patients Recruiting
sirolimus 0468H1-407 Graft Vs Host Disease, Kidney Transplantation, Skin Neoplasms, kidney transplantation, Study Evaluating Sirolimus in Non-Melanoma Skin Cancer in Kidney Transplant Recipients Phase 4 Completed
EKB-569 3095A1-200 Colorectal Neoplasms, Colonic Neoplasms, Rectal Neoplasms, Study evaluating EKB-569 in Advanced Colorectal Cancer Phase 2 No longer recruiting
TTI-237 3162K1-101 Neoplasms, Study Evaluating TTI-237 in Advanced Malignant Solid Tumors Phase 1 Terminated
CMD-193 3152K1-100 Neoplasms, study evaluating CMD-193 in advanced malignant solid tumors Phase 1 No longer recruiting
HKI-272 3144A1-203 Advanced Breast Cancer, Advanced Malignant Solid Tumors, Breast Neoplasms, A Phase I/II Study of HKI-272 in Combination with Paclitaxel in Subjects with Advanced Solid Tumors and Breast Cancer Phase 1/Phase 2 Active, not recruiting
temsirolimus 3066A1-132 Prostatic Neoplasms, An open label Exploratory Study in Newly Diagnosed Prostate Cancer Patients N/A Completed
MST-997 3161K1-101 Neoplasms, Study evaluating MST-997 in Advanced Malignant Solid Tumors Phase 1 Terminated
Letrozole / CCI-779 3066A1-204 Breast Neoplasms, Study evaluating CCI-779 in Breast Neoplasms Phase 2 Active, not recruiting
SKI-606 3160A2-201 Breast Neoplasms, Neoplasm Metastasis, Study Evaluating SKI-606 in Subjects with Breast Cancer Phase 2 Active, not recruiting
Temsirolimus (CCI-779) for 34 months 3066A1-303 Breast Neoplasms, Neoplasm Metastasis, Study evaluating CCI-779 and Letrozole in Post-menopausal Women with Breast Cancer Phase 3 Terminated

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The content on this page summarizes current scientific and medical research being conducted by Wyeth Pharmaceuticals. The intervention used in this study is investigational and is not available commercially. The safety and efficacy of this intervention has not been determined and this intervention has not been approved by FDA. No promotional claims about the products or product indications listed here should be inferred.

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