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Aspire Biopharma Holdings, Inc.

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Key Metrics

Previous Close
$7.90
52-Week Range
$0.11 – $23.80
Market Cap
$10.97M
P/E (TTM)
EPS (TTM)
-6.66
Dividend Yield
Advanced Metrics
Price/Book
0.86
PEG Ratio
Return on Equity
-1032.14%
Return on Assets
60.58%
Gross Margin
-25.04%
Operating Margin
-3880.58%
Profit Margin
0.00%
Current Ratio
7.99
Debt/Equity
Total Debt
$0.00
Free Cash Flow
$7.43M
Revenue Growth
Earnings Growth
Enterprise Value
$-1.20M

Market Snapshot

About

Aspire Biopharma Holdings operates as an early-stage biopharmaceutical company focused on developing innovative therapies for cancer and other serious diseases using novel approaches targeting tumor metabolism and immune system modulation. Headquartered in Taipei, Taiwan, the company advances drug candidates identified through partnerships with academic researchers and biotechnology collaborators, in-licensing promising compounds for clinical development and potential commercialization. Aspire Biopharma's pipeline includes small molecule therapeutics and immunotherapy approaches targeting specific cancer pathways including metabolic vulnerabilities distinguishing cancer cells from normal cells, potentially offering improved efficacy with reduced toxicity compared to conventional chemotherapies. The company operates with a capital-efficient business model focusing investment on clinical development while partnering with contract research organizations and manufacturing partners rather than building extensive internal infrastructure. Aspire Biopharma completed reverse merger transactions enabling public listing and capital raising to fund clinical trials advancing lead candidates through regulatory approval pathways. The company's development strategy emphasizes pursuing orphan drug designations and breakthrough therapy designations from regulatory agencies which can accelerate development timelines and provide market exclusivity benefits upon approval. Aspire Biopharma faces typical early-stage biotechnology risks including clinical trial uncertainties, substantial capital requirements for advancing programs through expensive Phase 2 and Phase 3 studies, and competitive pressures from established pharmaceutical companies and well-funded biotechnology firms pursuing similar cancer targets.