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Spots Global Cancer Trial Database for First-in-human Study of DS-1062a for Advanced Solid Tumors (TROPION-PanTumor01)

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Trial Identification

Brief Title: First-in-human Study of DS-1062a for Advanced Solid Tumors (TROPION-PanTumor01)

Official Title: Phase 1, Two-part, Multicenter, Open-label, Multiple Dose, First-in-human Study of DS-1062a in Subjects With Advanced Solid Tumors (TROPION-PanTumor01)

Study ID: NCT03401385

Study Description

Brief Summary: This study is one single group of participants with non-small cell lung cancer (NSCLC) who have not been cured by other treatments. It is the first time the drug has been used in humans. There will be two parts and a sub-study. The primary purpose of the parts are: * Dose Escalation: To investigate the safety and tolerability and to determine the maximum tolerated dose (MTD) and the recommended dose for expansion (RDE) of DS-1062a * Dose Expansion: To investigate the safety and tolerability of DS-1062a in additional solid tumors This study is expected to last approximately 6 years from the time the first participant is enrolled to the time the last subject is off the study. Study sites are located in both the United States and Japan. The number of treatment cycles is not fixed in this study. Participants who continue to benefit from the study treatment may continue, unless: * they withdraw * their disease gets worse * they experience unacceptable side effects. The primary purpose of the sub-study is to compare the effectiveness of steroid versus non-steroid mouthwash as prophylaxis against oral mucositis/stomatitis in participants receiving DS-1062a. The sub-study is a randomized study that will include approximately 76 participants enrolling into the Dose Expansion part.

Detailed Description: The dosage strength will change during the study but all participants will receive the same study drug. So the study is not a true 2-arm study, it is a 2-part study. In both parts, participants with pathologically documented unresectable advanced NSCLC and triple negative breast cancer (TNBC) who have been refractory to or relapsed from standard treatment or for which no standard treatment is available, will be enrolled. In Dose Expansion, additional indications (hormone receptor \[HR\]-positive human epidermal growth factor receptor 2 \[HER2\]-negative breast cancer, HR-positive HER2-low breast cancer, HER2-positive breast cancer, small cell lung cancer \[SCLC\], endometrial cancer, pancreatic adenocarcinoma, HER2-negative gastric/gastroesophageal junction \[GEJ\] cancer, esophageal cancer, head and neck squamous cell carcinoma \[HNSCC\], transitional cell carcinoma of the urothelium, colorectal cancer \[CRC\], platinum-resistant ovarian cancer, platinum-sensitive ovarian cancer, cervical cancer, and castration-resistant prostate cancer \[CRPC\]) may be evaluated, if the study treatment demonstrates acceptable safety, tolerability and efficacy in NSCLC participants. After the primary analysis, the main (registered) study will be considered complete, but data will be collected from participants who continue receiving study drug. In the sub-study, the additional indications listed for Dose Expansion (except for head and neck cancer) may be evaluated.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

University of California, Los Angeles, Los Angeles, California, United States

Johns Hopkins Sibley Memorial Hospital, Washington, District of Columbia, United States

Winship Cancer Institute of Emory University, Atlanta, Georgia, United States

Johns Hopkins University, Baltimore, Maryland, United States

Massachusetts General Hospital, Boston, Massachusetts, United States

Dana-Farber Cancer Institute, Boston, Massachusetts, United States

Tisch Cancer Institute, Icahn School of Medicine, New York, New York, United States

Memorial Sloan-Kettering Cancer Center, New York, New York, United States

Sarah Cannon Research Institute, Nashville, Tennessee, United States

MD Anderson Cancer Center, Houston, Texas, United States

Next Oncology, San Antonio, Texas, United States

START Oncology, San Antonio, Texas, United States

Virginia Cancer Specialists, Fairfax, Virginia, United States

Aichi Cancer Center, Nagoya, Aichi, Japan

The Cancer Institute Hospital of Japanese Foundation For Cancer Research, Koto-Ku, Tokyo, Japan

Showa University Hospital, Shinagawa-Ku, Tokyo, Japan

National Cancer Center Hospital, Chuo-Ku, , Japan

National Cancer Center Hospital East, Kashiwa, , Japan

Contact Details

Name: Global Team Leader

Affiliation: Daiichi Sankyo

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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