Safety, PK and Efficacy of ONC-392 in Monotherapy and in Combination of Anti-PD-1 in Advanced Solid Tumors and NSCLC (PRESERVE-001)

Complete Title: Safety, Pharmacokinetics (PK), and Efficacy of ONC-392 as a Single Agent and in Combination With Pembrolizumab in Advanced Solid Tumors and NSCLC: An Open Label Phase IA/IB Study.
Trial Phase: I/II
Investigator: Tina Rodriguez

This is a First-in-Human Phase IA/IB/II open label dose escalation study of intravenous (IV) administration of ONC-392, a humanized anti-CTLA4 IgG1 monoclonal antibody, as single agent and in combination with pembrolizumab in participants with advanced or metastatic solid tumors and non-small cell lung cancers.

Keywords:
  • Breast Cancer
  • Cervical Cancer
  • Esophageal Cancer
  • Gastric Cancer
  • Head and Neck Cancer
  • Melanoma
  • Ovarian Cancer
  • Pancreatic Cancer
  • Prostate Cancer
  • Renal Cancer
  • Salivary Gland Cancer
  • Sarcoma
  • Lung Carcinoma, Non-Small-Cell (NSCLC)
  • Colorectal Neoplasms
  • Lung Carcinoma, Small-Cell
  • Urothelial Cancer
  • Gastroesophageal Junction Cancer
  • Advanced Solid Tumors
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Adult
I/II
Tina Rodriguez
RG1122874
NCT04140526
Safety, Pharmacokinetics (PK), and Efficacy of ONC-392 as a Single Agent and in Combination With Pembrolizumab in Advanced Solid Tumors and NSCLC: An Open Label Phase IA/IB Study.
Breast Cancer
Cervical Cancer
Esophageal Cancer
Gastric Cancer
Head and Neck Cancer
Melanoma
Ovarian Cancer
Pancreatic Cancer
Prostate Cancer
Renal Cancer
Salivary Gland Cancer
Sarcoma
Lung Carcinoma, Non-Small-Cell (NSCLC)
Colorectal Neoplasms
Lung Carcinoma, Small-Cell
Urothelial Cancer
Gastroesophageal Junction Cancer
Advanced Solid Tumors