BioCardia, Inc. (BCDA)
| Market Cap | 10.48M -27.5% |
| Revenue (ttm) | n/a |
| Net Income | -7.78M |
| EPS | -0.95 |
| Shares Out | 11.37M |
| PE Ratio | n/a |
| Forward PE | n/a |
| Dividend | n/a |
| Ex-Dividend Date | n/a |
| Volume | 110,400 |
| Open | 0.9300 |
| Previous Close | 0.9003 |
| Day's Range | 0.9100 - 0.9325 |
| 52-Week Range | 0.8404 - 2.4500 |
| Beta | 0.55 |
| Analysts | Strong Buy |
| Price Target | 15.50 (+1,582.22%) |
| Earnings Date | May 15, 2026 |
About BCDA
BioCardia, Inc., a clinical-stage regenerative medicine company, develops cellular and cell-derived therapeutics for cardiovascular and pulmonary diseases in the United States. The company’s lead product candidate is CardiAMP, an autologous mononuclear cell therapy system in Phase III clinical trial for the treatment of ischemic heart failure with reduced ejection fraction and refractory angina resulting from chronic myocardial ischemia. It also provides CardiALLO, an allogeneic mesenchymal stem cell therapy which is in phase II for ischemic he... [Read more]
Financial Performance
Financial StatementsAnalyst Summary
According to 2 analysts, the average rating for BCDA stock is "Strong Buy." The 12-month stock price target is $15.5, which is an increase of 1,582.22% from the latest price.
News
BioCardia Announces CardiAMP Chronic Myocardial Ischemia Trial Results Presented at EuroPCR Showed Durable Improvements in Exercise Tolerance with Reduced Angina Frequency
– Positive CardiAMP CMI Trial open-label cohort results demonstrated opportunity for locally delivered cell therapy to enhance therapeutic options for patients with severely symptomatic refractory ang...
BioCardia Transcript: A.G.P.'s Annual Virtual Healthcare Conference
Barinthus Biotherapeutics is advancing its SNAP-TI platform for autoimmune diseases, with VTP-1000 in phase I for celiac disease and two diabetes assets from Clywedog expected post-merger. Key data readouts are anticipated in the second half of 2024 and 2027.
BioCardia Earnings Call Transcript: Q1 2026
CardiAMP cell therapy achieved key regulatory milestones in Japan and the U.S., with strong clinical data supporting efficacy and safety. Expenses and net loss decreased year-over-year, and the company is preparing for a major market entry in Japan with a $400M opportunity.
BioCardia Earnings release: Q1 2026
BioCardia released its Q1 2026 earnings on May 15, 2026, summarizing the period's financial results.
BioCardia Quarterly report: Q1 2026
BioCardia has published its Q1 2026 quarterly earnings report on May 15, 2026.
BioCardia Reports First Quarter 2026 Business Highlights and Financial Results
SUNNYVALE, Calif., May 15, 2026 (GLOBE NEWSWIRE) -- BioCardia, Inc. [Nasdaq: BCDA], a global leader in cellular and cell-derived therapeutics for the treatment of cardiovascular and pulmonary diseases...
BioCardia Slides: Corporate presentation
BioCardia has posted slides in relation to its latest quarterly earnings report, which was published on May 13, 2026.
BioCardia to Host Q1 2026 Financial Results and Corporate Update Conference Call on May 15, 2026
SUNNYVALE, Calif., May 11, 2026 (GLOBE NEWSWIRE) -- BioCardia®, Inc. [NASDAQ:BCDA], a developer of cellular and cell-derived therapeutics for the treatment of cardiovascular and pulmonary diseases, to...
BioCardia provides update on Helix pre-submission meeting with FDA
BioCardia (BCDA) announced the outcome of its pre-submission meeting with FDA on the Helix Transendocardial Delivery Catheter System. FDA agreed that there are two pathways for Helix marketing clearan...
BioCardia Slides: Corporate presentation
BioCardia has posted slides in relation to its latest quarterly earnings report, which was published on April 28, 2026.
BioCardia reports ‘positive’ outcome in consult with Japan’s PMDA for CardiAMP
BioCardia (BCDA) reported a positive outcome in its formal clinical consultation with Japan’s Pharmaceutical and Medical Device Agency, PMDA. PMDA has determined that the clinical safety and efficacy ...
BioCardia and Japan PMDA Align on Acceptability of CardiAMP Clinical Data to Support Regulatory Approval in Ischemic Heart Failure
SUNNYVALE, Calif., April 20, 2026 (GLOBE NEWSWIRE) -- BioCardia®, Inc. [Nasdaq: BCDA], a global leader in cellular and cell-derived therapeutics for the treatment of cardiovascular and pulmonary disea...
BioCardia files request for meeting with FDA to discuss CardiAMP pathway
BioCardia (BCDA) reported submission to FDA of the CardiAMP HF clinical study data and on its plans to meet with the FDA to discuss the accelerated approval pathway for the…
BioCardia Earnings Call Transcript: Q4 2025
Clinical and financial progress continues, with phase III CardiAMP HF data showing significant benefits in key subgroups and regulatory submissions imminent in the US and Japan. Expenses rose modestly, cash burn remains steady, and multiple near-term catalysts are expected.
BioCardia Earnings release: Q4 2025
BioCardia released its Q4 2025 earnings on March 24, 2026, summarizing the period's financial results.
BioCardia Annual report: Q4 2025
BioCardia has published its Q4 2025 annual report on March 24, 2026.
BioCardia Reports 2025 Business Highlights and Financial Results
SUNNYVALE, Calif., March 24, 2026 (GLOBE NEWSWIRE) -- BioCardia, Inc. [Nasdaq: BCDA], a global leader in cellular and cell-derived therapeutics for the treatment of cardiovascular and pulmonary diseas...
BioCardia to Host 2025 Financial Results and Corporate Update Conference Call on March 24, 2026
SUNNYVALE, Calif., March 19, 2026 (GLOBE NEWSWIRE) -- BioCardia®, Inc. [NASDAQ:BCDA], a developer of cellular and cell-derived therapeutics for the treatment of cardiovascular and pulmonary diseases, ...
BioCardia’s pre-submission package for Helix catheter approved by FDA
BioCardia (BCDA) announced the FDA has accepted its pre-submission package for the approval of its Helix Transendocardial Delivery Catheter intended for intramyocardial therapeutic and diagnostic agen...
BioCardia reports results from Phase III trial for ischemic heart failure
BioCardia (BCDA) reported late breaking echocardiography results from its Phase III clinical trial for ischemic heart failure of reduced ejection fraction, which affects millions of patients in the Un...
BioCardia files pre-submission for FDA approval of Helix catheter
BioCardia (BCDA) completed its Pre-Submission to FDA under its Q-Submission program for the approval of its Helix Transendocardial Delivery Catheter for intramyocardial therapeutic and diagnostic agen...
BioCardia Files Pre-Submission for FDA Approval of Helix™ Transendocardial Delivery Catheter for Therapeutic and Diagnostic Agent Delivery to the Heart
SUNNYVALE, Calif., Feb. 10, 2026 (GLOBE NEWSWIRE) -- BioCardia, Inc. [Nasdaq: BCDA], a developer of cellular and cell-derived therapeutics for the treatment of cardiovascular and pulmonary diseases, t...
BioCardia completed third preliminary clinical consultation with Japan’s PMDA
BioCardia (BCDA) announces it has completed a third preliminary clinical consultation with Japan’s Pharmaceutical and Medical Device Agency, PMDA, on CardiAMP Cell Therapy intended for treatment of He...
BioCardia Cell Therapy for Ischemic Heart Failure to Progress to Formal Clinical Consultation with Japan PMDA
SUNNYVALE, Calif., Dec. 16, 2025 (GLOBE NEWSWIRE) -- BioCardia®, Inc. [NASDAQ: BCDA], a developer of cellular and cell-derived therapeutics for the treatment of cardiovascular and pulmonary diseases, ...
BioCardia appoints Slosman to its Board of Directors
BioCardia (BCDA) announced the election of Marvin Slosman to its Board of Directors, effective December 2, 2025. Dr. Richard Krasno, who has served on the Board since 2016, has completed…