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Bicara Therapeutics/$BCAX

1D1W1M3M6MYTD1Y5YMAX

About Bicara Therapeutics

Bicara Therapeutics Inc is a clinical-stage biopharmaceutical company bringing transformative bifunctional therapies to patients with solid tumors. Its program ficerafusp alfa is a bifunctional antibody that combines two clinically validated targets, an epidermal growth factor receptor, or EGFR, directed monoclonal antibody with a domain that binds to human transforming growth factor beta, or TGF-b. The company's goal is to build a fully integrated, commercial-stage biopharmaceutical company that develops important therapies for people living with cancer, starting with ficerafusp alfa.
Ticker
$BCAX
Sector
Health
Primary listing
NASDAQ
Employees
103

BCAX Metrics

BasicAdvanced
$1.2B
-
-$3.11
-0.82
-

What the Analysts think about BCAX

Analyst ratings (Buy, Hold, Sell) for Bicara Therapeutics stock.
Analyst projections of the future price of Bicara Therapeutics stock.

Bulls say / Bears say

In a 28-patient HPV-negative subgroup, ficerafusp alfa plus pembrolizumab produced a 54% confirmed response rate, including 21% complete responses. Median response duration was 21.7 months, suggesting some patients may benefit for a long time. (Journal of Clinical Oncology)
Longer follow-up showed an estimated three-year survival rate of 31% in the 1,500mg weekly cohort, which Bicara said was about twice the rate in a retrospective pembrolizumab comparison. If confirmed in the pivotal trial, this could support a meaningful treatment benefit. (GlobeNewswire)
Bicara reported $497.3 million in cash and marketable securities at the end of June 2026, with a projected runway into the first half of 2029. That gives it funding to advance its pivotal study and other development work without an immediate need to raise more capital. (GlobeNewswire)
The encouraging response and survival figures come from small early-stage cohorts, while the three-year comparison uses historical rather than randomised control data. The pivotal study still needs to show that the benefit holds up against pembrolizumab in a controlled trial. (Journal of Clinical Oncology, GlobeNewswire)
Treatment burden could limit use: 45% of patients in the published cohort had a severe treatment-related side effect, 48% had treatment interruptions, and 12% stopped ficerafusp alfa because of side effects. These rates will need to be weighed against the treatment's benefit in larger studies. (Journal of Clinical Oncology)
The pivotal trial is expected to be substantially enrolled only by the end of 2026, with an interim readout planned for mid-2027. That leaves investors exposed to further execution risk and a long wait before randomised evidence can validate the early results. (GlobeNewswire)
Data summarised monthly by Lightyear AI. Last updated on 7 Oct 2026.

BCAX Financial Performance

Revenues and expenses
Income statement
QuarterlyAnnual
Q3 24
QoQ growth
Revenue
Net income
Profit margin

BCAX Earnings Performance

Company profitability
Earnings per share
QuarterlyAnnual
Q4 23
Q1 24
Q2 24
Q3 24
Q4 24
Actual
Expected
Surprise
Data displayed above is indicative only and its accuracy or completeness is not guaranteed. Actual execution price may vary. Past performance is not indicative of future results. Your return may be affected by currency fluctuations and applicable fees and charges. Capital at risk.
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