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Spots Global Cancer Trial Database for A Study of Amivantamab Subcutaneous (SC) Administration for the Treatment of Advanced Solid Malignancies

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Trial Identification

Brief Title: A Study of Amivantamab Subcutaneous (SC) Administration for the Treatment of Advanced Solid Malignancies

Official Title: An Open-label, Multicenter, Dose Escalation Phase 1b Study to Assess the Safety and Pharmacokinetics of Subcutaneous Delivery of Amivantamab, a Human Bispecific EGFR and cMet Antibody for the Treatment of Advanced Solid Malignancies

Study ID: NCT04606381

Study Description

Brief Summary: The purpose of this study is to assess the feasibility of subcutaneous (SC) administration of amivantamab based on safety and pharmacokinetics and determine a dose, dose regimen and formulation for amivantamab SC delivery.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Cedars Sinai Medical Center, West Hollywood, California, United States

Community Health Network, Indianapolis, Indiana, United States

Langone Health at NYC University, NYU School of Medicine, New York, New York, United States

Providence Portland Medical Center, Portland, Oregon, United States

Sarah Cannon Research Institute, Nashville, Tennessee, United States

University Health Network, Toronto, Ontario, Canada

Chungbuk National University Hospital, Cheongju-si, , Korea, Republic of

Seoul National University Bundang Hospital, Seongnam-si, , Korea, Republic of

Severance Hospital Yonsei University Health System, Seoul, , Korea, Republic of

Samsung Medical Center, Seoul, , Korea, Republic of

The Christie Nhs Foundation Trust, Manchester, , United Kingdom

Royal Marsden Hospital, Sutton, , United Kingdom

Contact Details

Name: Janssen Research & Development, LLC Clinical Trial

Affiliation: Janssen Research & Development, LLC

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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