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Generated: February 18, 2019

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CLINICAL TRIALS PROFILE FOR COTELLIC

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Clinical Trials for Cotellic

Trial ID Title Status Sponsor Phase Summary
NCT01928394 A Study of Nivolumab by Itself or Nivolumab Combined With Ipilimumab in Patients With Advanced or Metastatic Solid Tumors Recruiting Bristol-Myers Squibb Phase 1/Phase 2 To investigate the safety and efficacy of Nivolumab as a single agent or in combination with Ipilimumab in 6 tumor types - triple-negative breast cancer (TNBC), gastric cancer (GC), pancreatic adenocarcinoma (PC), small cell lung cancer (SCLC), bladder cancer (BC), and ovarian cancer (OC). A combination of Nivolumab with Ipilimumab and Cobimetinib is also investigated in PC.
NCT02060188 A Study of Nivolumab and Nivolumab Plus Ipilimumab in Recurrent and Metastatic Colon Cancer (CheckMate 142) Recruiting Bristol-Myers Squibb Phase 1/Phase 2 The purpose of this study is to examine if Nivolumab alone, Nivolumab in combination with Ipilimumab, or Nivolumab in combination with Ipilimumab and Cobimetinib will demonstrate a meaningful objective response rate in patients with recurrent and metastatic colon cancer who also have a specific biomarker in their tumors.
NCT02091141 A Study Evaluating Herceptin/Perjeta, Tarceva, Zelboraf/Cotellic, and Erivedge Treatment Targeted Against Certain Mutations in Cancer Patients Recruiting Genentech, Inc. Phase 2 This is a multicenter, non-randomized, open-label study designed to evaluate four treatment regimens in patients with advanced cancer for whom there is no available, beneficial treatment. Patients with HER2 overexpression, amplification, or -activating mutation will be treated with Herceptin/Perjeta; those with epidermal growth factor receptor (EGFR), with Tarceva; those with BRAF-activating mutation, with Zelboraf/Cotellic; and those with Hedehog pathway potentially clinically relevant mutation, with Erivedge. Treatment will continue until disease progression or unacceptable toxicity occurs. Study is expected to last up to 5 years.
NCT03101254 LY3022855 With BRAF/MEK Inhibition in Patients With Melanoma Recruiting Eli Lilly and Company Phase 1/Phase 2 This research study is studying a combination of targeted therapies as a possible treatment for advanced melanoma that was found to have a BRAF V600E or BRAF V600K genetic mutation The interventions involved in this study are: - LY3022855 - Vemurafenib - Cobimetinib
Trial ID Title Status Sponsor Phase Summary

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Clinical Trial Conditions for Cotellic

Condition Name

Condition Name for Cotellic
Intervention Trials
Non-small Cell Lung Cancer 1
BRAF V600 Mutation 1
Recurrent Cholangiocarcinoma 1
Malignant Melanoma Stage IV 1
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Condition MeSH

Condition MeSH for Cotellic
Intervention Trials
Melanoma 4
Carcinoma, Non-Small-Cell Lung 2
Neoplasm Metastasis 2
Breast Neoplasms 1
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Clinical Trial Locations for Cotellic

Trials by Country

Trials by Country for Cotellic
Location Trials
United States 70
Spain 4
United Kingdom 4
Germany 3
Australia 3
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Trials by US State

Trials by US State for Cotellic
Location Trials
Tennessee 5
Massachusetts 5
California 4
Texas 4
Oregon 4
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Clinical Trial Progress for Cotellic

Clinical Trial Phase

Clinical Trial Phase for Cotellic
Clinical Trial Phase Trials
Phase 2 6
Phase 1/Phase 2 6
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Clinical Trial Status

Clinical Trial Status for Cotellic
Clinical Trial Phase Trials
Recruiting 7
Not yet recruiting 5
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Clinical Trial Sponsors for Cotellic

Sponsor Name

Sponsor Name for Cotellic
Sponsor Trials
National Cancer Institute (NCI) 3
Genentech, Inc. 3
Hoffmann-La Roche 3
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Sponsor Type

Sponsor Type for Cotellic
Sponsor Trials
Industry 9
Other 5
NIH 3
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Serving hundreds of leading biopharmaceutical companies globally:

Dow
Chubb
Cipla
Queensland Health
Chinese Patent Office
Citi
QuintilesIMS
Medtronic
Moodys

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