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Spots Global Cancer Trial Database for Rollover Study for Continued Safety and Tolerability in Subjects Treated With Spartalizumab Alone or in Combination With Other Study Treatments

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Trial Identification

Brief Title: Rollover Study for Continued Safety and Tolerability in Subjects Treated With Spartalizumab Alone or in Combination With Other Study Treatments

Official Title: An Open-label, Multi-center Rollover Protocol for Continued Characterization of Safety and Tolerability for Subjects Who Have Participated in a Novartis-sponsored Spartalizumab Study as Single Agent or in Combination With Other Study Treatments

Study ID: NCT04058756

Interventions

PDR001

Study Description

Brief Summary: The purpose of this study is to continue to assess safety and tolerability, and to allow continued access to study treatment for subjects already receiving spartalizumab as single agent or in combination with other study treatments.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Columbia University Medical Center New York Presbyterian, New York, New York, United States

Providence Portland Medical Center, Portland, Oregon, United States

MD Anderson Cancer Center Uni of Te MDACC, Houston, Texas, United States

Novartis Investigative Site, Leuven, , Belgium

Novartis Investigative Site, Liege, , Belgium

Novartis Investigative Site, Toronto, Ontario, Canada

Novartis Investigative Site, Montreal, Quebec, Canada

Novartis Investigative Site, Guangzhou, Guangdong, China

Novartis Investigative Site, Guangzhou, , China

Novartis Investigative Site, Brno, Czech Republic, Czechia

Novartis Investigative Site, Praha 4, , Czechia

Novartis Investigative Site, Lille, , France

Novartis Investigative Site, Lyon, , France

Novartis Investigative Site, Marseille, , France

Novartis Investigative Site, Marseille, , France

Novartis Investigative Site, Villejuif, , France

Novartis Investigative Site, Essen, , Germany

Novartis Investigative Site, Heidelberg, , Germany

Novartis Investigative Site, Jena, , Germany

Novartis Investigative Site, Ulm, , Germany

Novartis Investigative Site, High West, , Hong Kong

Novartis Investigative Site, Hong Kong, , Hong Kong

Novartis Investigative Site, Shatin New Territories, , Hong Kong

Novartis Investigative Site, Budapest, , Hungary

Novartis Investigative Site, Debrecen, , Hungary

Novartis Investigative Site, Debrecen, , Hungary

Novartis Investigative Site, Milano, MI, Italy

Novartis Investigative Site, Milano, MI, Italy

Novartis Investigative Site, Milano, MI, Italy

Novartis Investigative Site, Rozzano, MI, Italy

Novartis Investigative Site, Modena, MO, Italy

Novartis Investigative Site, Aviano, PN, Italy

Novartis Investigative Site, Siena, SI, Italy

Novartis Investigative Site, Napoli, , Italy

Novartis Investigative Site, Napoli, , Italy

Novartis Investigative Site, Seoul, , Korea, Republic of

Novartis Investigative Site, Seoul, , Korea, Republic of

Novartis Investigative Site, Leiden, , Netherlands

Novartis Investigative Site, Gdansk, , Poland

Novartis Investigative Site, Poznan, , Poland

Novartis Investigative Site, Barcelona, Catalunya, Spain

Novartis Investigative Site, Barcelona, Catalunya, Spain

Novartis Investigative Site, Hospitalet de LLobregat, Catalunya, Spain

Novartis Investigative Site, Valencia, Comunidad Valenciana, Spain

Novartis Investigative Site, Madrid, , Spain

Novartis Investigative Site, Madrid, , Spain

Novartis Investigative Site, Madrid, , Spain

Novartis Investigative Site, Zuerich, , Switzerland

Novartis Investigative Site, Taipei, , Taiwan

Novartis Investigative Site, Songkhla, Hat Yai, Thailand

Novartis Investigative Site, Bangkok, , Thailand

Novartis Investigative Site, Chiang Mai, , Thailand

Contact Details

Name: Novartis Pharmaceuticals

Affiliation: Novartis Pharmaceuticals

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

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