Study of Ridaforolimus (MK-8669) in Participants With Solid Tumors (MK-8669-003)(COMPLETED)
Phase 1 Completed
13 enrolled
Ridaforolimus in Treating Patients With Recurrent Metastatic and/or Locally Advanced Endometrial Cancer
Phase 2 Completed
35 enrolled
Ridaforolimus and Vorinostat in Treating Patients With Advanced Solid Tumors or Lymphoma
Phase 1 Completed
16 enrolled 7 charts
Ridaforolimus With Cetuximab: Adv Non-Small Cell Lung, Colorectal, Head & Neck Cancer
Phase 1 Terminated
12 enrolled 7 charts
MK-8669-037
Phase 1 Completed
23 enrolled 14 charts
MK-8669-064
Phase 2 Completed
80 enrolled 13 charts
MK-8669-056
Phase 1 Terminated
20 enrolled 10 charts
MK-8669-038
Phase 2 Terminated
7 enrolled 13 charts
A Study of Dalotuzumab + MK-2206, Dalotuzumab + MK-0752, and Dalotuzumab + Ridaforolimus Combination Therapies in Participants With Advanced Cancer (MK-0646-027)
Phase 1 Terminated
47 enrolled 12 charts
Carboplatin/Taxol/Ridaforolimus in Endometrial, Ovarian and Solids
Phase 1 Completed
24 enrolled
Study of Dalotuzumab Alone and With Ridaforolimus in Pediatric Participants With Advanced Solid Tumors (MK-8669-062 AM1)
Phase 1 Completed
21 enrolled
Ridaforolimus (AP23573/MK-8669) in Participants With Taxane-Resistant Androgen-Independent Prostate Cancer (AIPC)(MK-8669-017)
Phase 2 Completed
39 enrolled
Safety Study of Ridaforolimus in Patients With Advanced, Refractory or Recurrent Malignancies (MK-8669-001 AM5)(COMPLETED)
Phase 1 Completed
46 enrolled
Safety Study of AP23573 in Patients With Advanced, Refractory or Recurrent Malignancies (8669-013)(COMPLETED)
Phase 1 Completed
33 enrolled
Oral Deforolimus With Trastuzumab for Patients With HER2-positive Trastuzumab-Refractory Metastatic Breast Cancer (8669-009)
Phase 2 Completed
34 enrolled
Safety and Tolerability of Different Dose Combinations of Ridaforolimus With MK-2206 or MK-0752 for Participants With Advanced Cancer (MK-8669-049)
Phase 1 Completed
65 enrolled
Study of AP23573 in Patients With Relapsed or Refractory Hematologic Malignancies (8669-024)(COMPLETED)
Phase 2 Completed
57 enrolled
Bicalutamide and Ridaforolimus in Men With Prostate Cancer (MK-8669-002)
Phase 2 Completed
22 enrolled
Safety, Tolerability and Maximum Tolerated Dose of Oral AP23573 in Combination With Doxorubicin (8669-015)
Phase 1 Completed
37 enrolled
Clinical Trial of Ridaforolimus Compared to Progestin or Chemotherapy for Advanced Endometrial Carcinoma (MK-8669-007 AM6)
Phase 2 Completed
130 enrolled
Phase II Study of Ridaforolimus (MK-8669) With Metastatic Bone or Soft-tissue Sarcoma Patients (MK-8669-030 AM1)
Phase 2 Completed
50 enrolled
Effect of Ridaforolimus on the Pharmacokinetics of Midazolam (Study MK-8669-044)
Phase 1 Completed
16 enrolled
AP23573 in Female Adult Patients With Recurrent or Persistent Endometrial Cancer (8669-019)(COMPLETED)
Phase 2 Completed
45 enrolled
Study of AP23573/MK-8669 (Ridaforolimus), A Mammalian Target of Rapamycin (mTOR) Inhibitor, in Participants With Advanced Sarcoma (MK-8669-018 AM1)(COMPLETED)
Phase 2 Completed
216 enrolled
SUCCEED
Phase 3 Completed
711 enrolled
Trial of Deforolimus in Combination With Bevacizumab for Patients With Advanced Cancers (8669-010)(COMPLETED)
Phase 1 Completed
17 enrolled
Study of Oral Ridaforolimus (AP23573, MK-8669) to Treat Patients With Refractory or Advanced Malignancies (MK-8669-016 AM4)(COMPLETED)
Phase 1 Completed
147 enrolled
A Study of Ridaforolimus in Non-Small Cell Lung Cancer (NSCLC) Patients With Kirsten Rat Sarcoma Viral Oncogene Homolog (KRAS) Mutations (MK-8669-021 AM1)
Phase 2 Terminated
80 enrolled
The Growth Factor Signature (GFS) as an Intermediate Biomarker of Response for Development of PI3K-Pathway Inhibitors in Patients With Breast Cancer (MK-8669-050)
Phase 1 Completed
63 enrolled