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Reviva Announces Letter to Shareholders

  • Reviva Pharmaceuticals Holdings, Inc. announced a shareholder letter from CEO Laxminarayan Bhat, Ph.D. dated April 15, 2026.
  • The company closed a $10 million financing on March 20, 2026, to strengthen its balance sheet.
  • Following the capital raise, Reviva reported approximately $23 million in cash and cash equivalents, which is expected to fund operations through Q1 2027.
  • Reviva is evaluating strategic alternatives to maximize the value of its lead candidate, brilaroxazine.
  • The company plans to extend patent life and commercial exclusivity for brilaroxazine potentially through 2046.
  • Reviva filed a composition of matter patent application for a new form of brilaroxazine and is pursuing an accelerated review process.
  • The company intends to seek FDA alignment mid-year 2026 to switch the active pharmaceutical ingredient in the upcoming second Phase 3 trial.
  • Preparations for the second Phase 3 trial, RECOVER-2, are underway with trial activities expected to begin in Q2 2026.
  • Patient enrollment for RECOVER-2 in the United States is scheduled for Q3 2026, with study completion expected in Q4 2027.
  • The FDA has already cleared the protocol for the RECOVER-2 trial in schizophrenia.
  • Brilaroxazine previously met all primary and secondary endpoints in the global Phase 3 RECOVER trial for schizophrenia.
  • Reviva aims to develop brilaroxazine for additional neuropsychiatric indications including bipolar disorder, major depressive disorder, and ADHD.
  • Brilaroxazine holds Orphan Drug Designation from the FDA for pulmonary arterial hypertension and idiopathic pulmonary fibrosis.