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Phase I/IIa, Open-label Multicenter Study to Assess the Safety, Tolerability, Pharmacokinetics, and Preliminary Antitumor Activity of PEN-221 in Patients With Somatostatin Receptor 2 Expressing Advanced Cancers, Including Gastroenteropancreatic or Lung or Thymus or Other Neuroendocrine Tumors or Small Cell Lung Cancer or Large Cell Neuroendocrine Carcinoma of the Lung

Summary

5/22/2018 NOTE: This trial is currently enrolling into the phase IIa cohorts. The purpose of this phase I/II study is to evaluate the safety and efficacy of PEN-221 in patients with SSTR2 expressing advanced gastroenteropancreatic (GEP) or lung or thymus or other neuroendocrine tumors or small cell lung cancer or large cell neuroendocrine carcinoma of the lung. Biomarker testing to determine if patient is eligible will be done during prescreening for the trial; however, reports performed within the last 6 months prior to enrollment are acceptable. Patients may contact Laura Mei or Leila Alland at clinical.information@tarveda.com for more information.

General Information

NCT#: NCT02936323
Study ID: PEN-221-001
Trial Phase: Phase I/II

Trial Sponsor: Tarveda Therapeutics
Therapies Used in This Trial: PEN-221

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