
Core Insights - Tempest Therapeutics has made significant progress in 2024, achieving key milestones in the development of its drug candidates, particularly Amezalpat (TPST-1120) for Hepatocellular Carcinoma (HCC) and TPST-1495 for Familial Adenomatous Polyposis (FAP) [2][3] Drug Development Progress - Amezalpat (TPST-1120) received both Orphan Drug and Fast Track designations from the FDA for the treatment of HCC [3] - The company has secured regulatory agreement with the FDA and EMA on the Phase 3 plan for Amezalpat and received a "Study May Proceed" letter for its pivotal Phase 3 trial [2][3] - Amezalpat demonstrated a six-month improvement in median overall survival when combined with atezolizumab and bevacizumab compared to the standard of care [3] - An agreement with Roche was announced to advance Amezalpat in combination therapy into a pivotal Phase 3 trial for first-line treatment of unresectable or metastatic HCC [3] - TPST-1495 received a "Study May Proceed" letter from the FDA for a Phase 2 trial targeting FAP, with data expected in 2026 [3][7] Financial Performance - For the year ended December 31, 2024, Tempest reported a net loss of $41.8 million, or $1.50 per share, compared to a net loss of $29.5 million, or $1.91 per share, in 2023 [7][11] - Research and development expenses increased to $28.5 million from $17.5 million in the previous year, primarily due to costs associated with the pivotal Phase 3 trial of Amezalpat [7][11] - The company ended 2024 with $30.3 million in cash and cash equivalents, down from $39.2 million at the end of 2023 [7][9] Corporate Developments - Tempest expanded its leadership team to enhance global clinical expertise, appointing new Vice Presidents for Quality Assurance and Regulatory Affairs [3]