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Spots Global Cancer Trial Database for Study of Single Agent CJM112, and PDR001 in Combination With LCL161 or CJM112 in Patients With Multiple Myeloma

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Study of Single Agent CJM112, and PDR001 in Combination With LCL161 or CJM112 in Patients With Multiple Myeloma

Official Title: Phase I/Ib, Multi-center, Open-label, Study of Single Agent CJM112, and PDR001 in Combination With LCL161 or CJM112 in Patients With Relapsed and/or Refractory Multiple Myeloma

Study ID: NCT03111992

Interventions

PDR001
CJM112
LCL161

Study Description

Brief Summary: The purpose of this study is to assess the safety, tolerability, and identify the recommended doses of single agent CJM112, and of CJM112 or LCL161 in combination with PDR001, in patients with relapsed and/or refractory multiple myeloma.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Mayo Clinic Arizona, Phoenix, Arizona, United States

Sarah Cannon Research Institute, Nashville, Tennessee, United States

Novartis Investigative Site, Freiburg, , Germany

Novartis Investigative Site, Heidelberg, , Germany

Novartis Investigative Site, Kiel, , Germany

Novartis Investigative Site, Milano, MI, Italy

Novartis Investigative Site, Salamanca, Castilla Y Leon, Spain

Novartis Investigative Site, Madrid, , Spain

Contact Details

Name: Novartis Pharmaceuticals

Affiliation: Novartis Pharmaceuticals

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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