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AVEO Pharmaceuticals, CANbridge AV-203 Licensing Deal Axed, AVEO Regains Ex-North American Rights

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AVEO Pharmaceuticals Inc’s (NASDAQ: AVEO) brief positive news of getting FDA approval for Tivozanib in relapsed kidney cancer this month was upset after its partner CANbridge Life Sciences voluntarily terminated the collaboration agreement.

  • The company said it would “regain its rights” to the investigational cancer med AV-203 outside North America from early September.
  • The deal was inked in 2016, with $1 million upfront and up to $133 million in milestone payments.
  • In August 2018, AVEO received a $2 million milestone payment from CANbridge for regulatory approval from the National Medical Products Administration in China for AV-203 investigational new drug application in esophageal squamous cell cancer.
  • AV-203 is an IgG1 antibody. To date, AVEO has completed a Phase 1 dose-escalation study of AV-203 in patients with advanced solid tumors (N=22).
  • On Friday, AVEO collaborated with Bristol-Myers Squibb Co (NYSE: BMY) to evaluate Fotivda (tivozanib) in combination with Opdivo (nivolumab) in advanced relapsed or refractory renal cell carcinoma following prior immunotherapy exposure.
  • Price Action: AVEO shares are up 0.08% at $12.45 in market trading hours on the last check Monday.
 

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Posted-In: cancerBiotech News Health Care Small Cap FDA General

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