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Spots Global Cancer Trial Database for Phase-II Study of Lu177DOTATOC in Adults With STTR(+)Pulmonary, Pheochromocytoma, Paraganglioma, Unknown Primary, Thymus NETs (PUTNET), or Any Other Non-.GEP-NET.

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Trial Identification

Brief Title: Phase-II Study of Lu177DOTATOC in Adults With STTR(+)Pulmonary, Pheochromocytoma, Paraganglioma, Unknown Primary, Thymus NETs (PUTNET), or Any Other Non-.GEP-NET.

Official Title: A Phase II, Non-Randomized, Open-Label, Single-center, Physician Sponsored Study to Determine the Safety and Effectiveness of Lu-177 DOTATOC in Adult Subjects With Somatostatin Receptor Expressing Pulmonary, Pheochromocytoma, paragangliomUnknown Primary, and Thymus Neuroendocrine Tumors (PUTNET) or Any Other Non-.GEP-NET.

Study ID: NCT04276597

Interventions

177Lu-DOTATOC

Study Description

Brief Summary: Determine the safety and effectiveness of Lu-177 DOTATOC in adult subjects with somatostatin receptor-expressing Pulmonary, Pheochromocytoma, Paraganglioma, Unknown primary, and Thymus neuroendocrine tumors or any other non-.GEP-NET. The treatment regimen will consist of 4 doses of 200 (±10%) mCi 177Lu-DOTATOC administered at 8+/- 1-week intervals.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Excel Diagnostics and Nuclear Oncology Center, Houston, Texas, United States

Contact Details

Name: Ebrahim Delpassand, MD

Affiliation: Excel Diagnostics and Nuclear Oncology Center

Role: PRINCIPAL_INVESTIGATOR

Name: Rodolfo Nunez, MD

Affiliation: Excel Diagnostics and Nuclear Oncology Center

Role: STUDY_DIRECTOR

Name: Afshin Shafie, MD

Affiliation: Excel Diagnostics and Nuclear Oncology Center

Role: STUDY_DIRECTOR

Name: Ayman Gaber, MD

Affiliation: Excel Diagnostics and Nuclear Oncology Center

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

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