BCDA

Biocardia Inc
NASDAQHEALTHCAREBIOTECHNOLOGY

Key Statistics

Market Cap
$14.29M
P/E Ratio
EPS
$-0.85
Beta
0.44
52W High
$2.42
52W Low
$0.78
50-Day MA
$1.02
200-Day MA
$1.23
Dividend Yield
Profit Margin
0.00%
Forward P/E
PEG Ratio
0.00

About Biocardia Inc

BioCardia, Inc., a clinical-stage regenerative medicine company, develops therapies for cardiovascular disease. The company is headquartered in San Carlos, California.

Official WebsiteUSAFY End: December

Fundamentals

Revenue (TTM)0
Gross Profit (TTM)$-4.67M
EBITDA$-7.80M
Operating Margin0.00%
Return on Equity-950.00%
Return on Assets-252.00%
Revenue/Share (TTM)$0.00
Book Value$-0.10
Price-to-Book12.35
Price-to-Sales (TTM)1985.81
EV/Revenue3111.7
EV/EBITDA-3.16
Quarterly Earnings Growth (YoY)0.00%
Quarterly Revenue Growth (YoY)-100.00%
Shares Outstanding$14.88M
Float$8.43M
% Insiders23.00%
% Institutions5.45%

Historical Volatility

HV 10-Day
104.62%
HV 20-Day
97.65%
HV 30-Day
95.31%
HV 60-Day
78.19%
HV Rank
86.9%

Volatility is currently expanding

Analyst Ratings

Consensus ($15.50 target)
2
Buy

Latest News

BioCardia Letter to Stockholders on 2026 Priorities and Strategic Opportunities

SUNNYVALE, Calif., June 18, 2026 (GLOBE NEWSWIRE) -- BioCardia®, Inc. [Nasdaq: BCDA], a global leader in cellular and cell-derived therapeutics for the treatment of cardiovascular and pulmonary diseases, today announced that the Company's Chief Executive Officer, Peter Altman, issued the following letter to shareholders.

GlobeNewsWire6/18/2026Neutral
FDA Confirms CardiAMP HF II May Support Premarket Approval of CardiAMP Cell Therapy for Ischemic HFrEF

SUNNYVALE, Calif., June 05, 2026 (GLOBE NEWSWIRE) -- BioCardia®, Inc. [Nasdaq: BCDA], a global leader in cellular and cell-derived therapeutics for the treatment of cardiovascular and pulmonary diseases, today announced receipt of FDA minutes from its Q-Sub Meeting with FDA Center for Biologics Evaluation and Research (CBER) on the CardiAMP Cell Therapy System for the treatment of ischemic heart failure of reduced ejection fraction (HFrEF).

GlobeNewsWire6/5/2026Neutral
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 angina and validate continued clinical development – Novel therapeutic approach targets a critically important unmet medical need for patients who have debilitated quality-of-life and have exhausted all available treatment options SUNNYVALE, Calif., May 21, 2026 (GLOBE NEWSWIRE) -- BioCardia, Inc. (NASDAQ: BCDA), a global leader in cellular and cell-derived therapeutics for the treatment of cardiovascular and pulmonary diseases, today announced the oral presentation of the results of the CardiAMP® Cell Therapy in Chronic Myocardial Ischemia Trial (CardiAMP CMI) preliminary open label cohort at EuroPCR, a leading interventional cardiovascular medicine conference held in Paris.

GlobeNewsWire5/21/2026Neutral
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, today reported financial results for the first quarter 2026 and filed its quarterly report on Form 10-Q for the three months ended March 31, 2026 with the Securities and Exchange Commission. The Company will also hold a conference call at 4:30 PM ET today in which it will discuss business highlights. Following management's formal remarks, there will be a question-and-answer session.

GlobeNewsWire5/15/2026Neutral
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 diseases, today 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 evidence for the CardiAMP® Cell Therapy in ischemic heart failure is likely sufficient to support market clearance.

GlobeNewsWire4/20/2026Neutral

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Data last updated: 7/9/2026