Held · Bookmarked
0 · 0
portfolios · users
Avg position size
—
of holders' portfolios
13F filers
1
institution
Market cap
$17.9M
15M shares
52-week range
$0.78 – $2.45
26% from low
Sector
BIOLOGICAL PRODUCTS, (NO DIAGNOSTIC SUBSTANCES)
Exchange
NASDAQ
CS
Borrow rate
44.25%
Hard to borrow
Click rows below (any statement) to add/remove series. Selection stays as you switch tabs.
| 2018 | 2019 | 2020 | 2021 | 2022 | 2023 | 2024 | 2025 | |
|---|---|---|---|---|---|---|---|---|
| Revenue | $625.0K | $710.0K | $145.0K | $1.0M | $1.4M | $477.0K | $58.0K | $0 |
| Cost of revenue | $517.0K | $358.0K | $4.0K | $640.0K | $8.8M | $7.7M | $4.4M | $505.0K |
| Gross profit | $108.0K | $352.0K | $141.0K | $375.0K | −$7.5M | −$7.2M | −$4.3M | −$505.0K |
| Gross margin | 17.3% | 49.6% | 97.2% | 36.9% | -553.4% | -1519.7% | -7463.8% | — |
| R&D | $8.5M | $8.6M | $9.8M | $8.6M | $8.8M | $7.7M | $4.4M | $5.0M |
| Operating income | −$14.1M | −$14.2M | −$15.5M | −$12.6M | −$11.9M | −$11.6M | −$8.0M | −$8.3M |
| EBITDA | −$13.9M | −$14.0M | −$14.4M | −$12.6M | −$11.8M | −$11.5M | −$7.9M | −$7.7M |
| Net income | −$14.0M | −$14.7M | −$15.0M | −$12.6M | −$11.9M | −$11.6M | −$7.9M | −$8.2M |
| Net margin | -2237.9% | -2071.7% | -10347.6% | -1243.4% | -880.7% | -2425.8% | -13700.0% | — |
| EPS (diluted) | -48.80 | -39.15 | -22.20 | -11.19 | -10.05 | -8.19 | -2.90 | -1.23 |
Annual figures · source: Financial Modeling Prep
| Year | Est. revenue | Est. EPS | EPS range | # Analysts |
|---|---|---|---|---|
| 2026 | $50000 | $-0.68 | $-0.68–$-0.68 | 1 |
| 2027 | $50000 | $-0.53 | $-0.53–$-0.53 | 1 |
| 2028 | $4M | $-0.41 | $-0.42–$-0.40 | 2 |
Forward consensus · source: Financial Modeling Prep
BioCardia Inc is a clinical-stage company developing cellular and cell-derived therapeutics for the treatment of cardiovascular and pulmonary diseases with unmet medical needs. Its two cell therapy platforms derived from the bone marrow. CardiAMP autologous mononuclear cell therapy platform is being for two clinical indications: ischemic heart failure with reduced ejection fraction (HFrEF) and refractory angina resulting from chronic myocardial ischemia (CMI). Its immunomodulatory allogeneic mesenchymal stem cell (MSC) therapy platform is being an off the shelf cell therapy for two clinical indications: the treatment of ischemic HFrEF (CardiALLO), which is actively enrolling, and acute respiratory distress syndrome (ARDS).
www.biocardia.comNo one on the platform currently holds BCDA.
| Institution | Shares | Reported |
|---|---|---|
| Renaissance Technologiesas of 2026-03-31 | 13,900 | $16.8K |
| Execution date | Ratio |
|---|---|
| 2024-05-30 | 1-for-15reverse |
| 2019-06-06 | 1-for-9reverse |
| 2017-11-03 | 1-for-12reverse |
| 2004-01-06 | 6-for-1 |
No one on the platform has traded BCDA yet.
| $5M |
| — |
| APVOAptevo Therapeutics Inc. | $4.55 | -0.66% | $10M | — |
| CELZCreative Medical Technology Holdings, Inc. | $1.20 | -40.00% | $3M | — |
Source: Financial Modeling Prep · peers by sector/industry
$BCDA Does anyone else understand the vast potential of a drug that can combat ischemic heart failure, the number one killer of both men and women worldwide? Naïve me? 
View on StockTwits ↗$BCDA Added shares on Friday & today…. only 2,935 shares away from hitting my phase 1. objective.
View on StockTwits ↗$BCDA I've been in SLS and looking for the next thing. is this worth it? anyone give me the lowdown?
View on StockTwits ↗@refloS After approval, I'll see where the SP is, and what the charts and experts are saying. But I kinda want to jump ship at that point and invest more money in $BCDA. That is up for FDA approval as well, and some are saying it will get up to $25
View on StockTwits ↗$BCDA there’s no real speculation or data on repeating the CardiAMP procedure. All their trials, including the ongoing Phase 3, treat it as a one-time, single-dose therapy. The two-year follow-up data showed durable benefits out to at least two years, and the company has highlighted that a single dose offers lasting effects. The autologous nature of the cells does preserve the option for future retreatment if needed, but BioCardia hasn’t studied or promoted repeat dosing. Their focus is on one minimally invasive procedure using the patient’s own bone marrow cells. No clinical data exists yet on how often, or even if, it should be repeated for better outcomes.
View on StockTwits ↗$BCDA in Japan. BioCardia isn’t running any clinical trials for CardiAMP there. Instead, they’re using data from their completed U.S. trials—including the Phase 3 CardiAMP Heart Failure study—to seek approval. Japan’s PMDA has been supportive, saying the existing foreign clinical data looks sufficient for a regulatory submission. The company plans to file their Shonin application in the fourth quarter of 2026, aiming for approval based on that U.S. data plus a post-marketing study in Japan. They’re targeting an initial subgroup of about 20,000 patients out of roughly 300,000 with ischemic heart failure in Japan. If approved, it could come with precedent reimbursement around $124,000 per procedure.
View on StockTwits ↗$BCDA It’s actively recruiting —the CardiAMP Heart Failure II trial is a confirmatory Phase 3 study targeting up to 250 patients with ischemic heart failure and reduced ejection fraction. It’s designed to enroll people with elevated NT-proBNP — the subgroup that showed the strongest benefits in the first Phase 3 trial. Yes, they modified it significantly. They narrowed the population to patients with active heart stress (elevated NT-proBNP), where the first trial showed an 86% relative risk reduction in mortality. They also replaced the six-minute walk test in the primary endpoint with a validated quality-of-life score (Minnesota Living with Heart Failure Questionnaire). That change alone would have made the endpoint statistically significant in this subgroup. (Continued in comment)
View on StockTwits ↗Recent $TICKER stream from stocktwits.com — refreshed every 5 minutes. Sentiment tags are self-reported by posters. Not investment advice.
Trading at 757.1× sales vs its 56.6× historical median P/S.
Fair value ≈ $0.09 · price $1.21 today
Fair-value line = the stock's median historical P/S × sales per share. Price below the orange line = cheap vs its own history; above = expensive. Not investment advice.
Click to see transaction details on SEC.gov. Form 4s cover trades by officers, directors, and 10%+ owners, due within 2 business days of the trade.