Tivantinib

Drug Profile

Tivantinib

Alternative Names: ARQ-197

Latest Information Update: 20 May 2017

Price : $50

At a glance

  • Originator ArQule
  • Developer ArQule; Daiichi Sankyo Company; Istituto Clinico Humanitas; Istituto Oncologico Veneto; Kyowa Hakko Kirin; National Cancer Institute (USA); National Institutes of Health (USA); SCRI Development Innovations
  • Class Antineoplastics; Pyrrolidinones; Quinolines; Small molecules
  • Mechanism of Action Proto oncogene protein c met inhibitors
  • Orphan Drug Status

    Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.

    Yes - Soft tissue sarcoma
  • New Molecular Entity Yes

Highest Development Phases

  • Phase III Hepatocellular carcinoma
  • Phase II Colorectal cancer; Head and neck cancer; Mesothelioma; Multiple myeloma; Prostate cancer; Renal cell carcinoma; Small cell lung cancer
  • Phase I/II Solid tumours
  • Discontinued Gastric cancer; Germ cell and embryonal neoplasms; Non-small cell lung cancer; Pancreatic cancer; Soft tissue sarcoma

Most Recent Events

  • 09 Mar 2017 ArQule has patent protection for tivantinib in US, Japan, the EU, South Korea, Singapore, Australia, China, Mexico, New Zealand, Philippines, Russia and South Africa (ArQule's form 10-K, filed in March 2017)
  • 09 Mar 2017 ArQule has patents pending for tivantinib in USA and countries outside USA (ArQule's form 10-K, filed in March 2017)
  • 17 Feb 2017 Daiichi Sankyo and ArQule complete the phase III METIV-HCC trial in Hepatocellular carcinoma (Inoperable/Unresectable, Monotherapy, Second-line therapy or greater) in Argentina, Australia, Austria, Belgium, Brazil, Canada, France, Germany, Italy, Netherlands, New Zealand, Portugal, Spain, Sweden, Switzerland, and USA
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