Bicara Therapeutics Logo
US0554771032
BCAX

Bicara Therapeutics

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Previsión

El precio objetivo medio de los analistas es de +27,98 (+31,30%). La mediana es de +30,07 (+41,11%).

Comprar
  6
Mantener
  3
Vender
  0

  • Bicara Therapeutics names new CEO and CFO and confirms trial progress

    Bicara Therapeutics has appointed Ryan Cohlhepp as CEO effective January 1, 2027; Dr. Claire Mazumdar will move into the role of vice chair and strategic advisor. Jenn Larson has been named CFO with immediate effect; additional management changes affect COO, CDO and business roles, and Greg Shiferman will join as chief legal officer effective August 31, 2026. The company reports progress in the regulatory FORTIFI-HN01 study for ficerafusp alfa and expects topline data from an interim analysis in mid-2027; the FORTIFI-FLEX study has also been initiated. In Q2 2026 Bicara posted a net loss of $55.4 million (prior year: $27.4 million) driven by higher R&D spending; cash and cash equivalents were $497.3 million as of June 30, 2026, which the company says funds operations through the first half of 2029. » Más en de.investing.com


  • Bicara Therapeutics hits record high of $29.92 after study updates

    Shares of Bicara Therapeutics rose to a new all-time high of $29.92, close to their 52-week high, up 221.6% year to date. The company reported expanded follow-up data on ficerafusp alfa plus pembrolizumab showing an estimated 3-year survival rate of about 31% at a 1500 mg dose. Analysts reiterated ratings: Citizens maintains "Market Outperform" with a $31.00 price target, Cantor Fitzgerald reaffirmed "Overweight", while InvestingPro flagged potential overvaluation and an overbought RSI. » Más en de.investing.com


  • Bicara Therapeutics shows 31% three‑year survival rate with Ficerafusp alfa plus pembrolizumab

    Extended follow‑up data from a phase 1/1b study show that with a weekly dose of 1500 mg Ficerafusp alfa combined with pembrolizumab, an estimated 31% of patients with recurrent/metastatic HPV‑negative squamous cell carcinoma of the head and neck survived at three years. The study of about 90 patients also showed varying response and overall response rates across the three dose cohorts; median progression‑free survival ranged from 6.9 to 12.7 months. Bicara plans a phase 3 continuation (FORTIFI‑HN01) with 1500 mg weekly and intends to start a study with a different dosing regimen in Q3 2026; the FDA has granted the combination Breakthrough Therapy designation. Investors reacted positively to the data, with the stock trading near its 52‑week high, while a fair‑value analysis suggests possible overvaluation. » Más en de.investing.com

Datos financieros de la empresa

En el último trimestre, Bicara Therapeutics tuvo unos ingresos de 0,00 y un beneficio neto de 48,57 Mio
(EUR) jun 2026
YoY
Ingresos 0,00 -
Beneficio bruto 0,00 -
Beneficio neto 48,57 Mio 109,04%
EBITDA 47,94 Mio 106,85%

Datos fundamentales

Métrica Valor
Capitalización bursátil
+1,40 Mrd
Número de acciones
65,70 Mio
Máximo/mínimo de 52 semanas
+26,62 - +8,84
Dividendos No
Beta
-0,75
Ratio P/E
8,01
Ratio PEG
+0,18
Ratio P/B
+3,60
Ratio P/S
0,00

Perfil de la empresa

Bicara Therapeutics Inc. ist ein biopharmazeutisches Unternehmen im klinischen Stadium, das bifunktionale Therapien für solide Tumore entwickelt. Sein führendes Programm ist Ficerafusp alfa, ein bifunktionaler Antikörper, der einen gegen den epidermalen Wachstumsfaktor-Rezeptor (EGFR) gerichteten monoklonalen Antikörper mit einer Domäne kombiniert, die an den menschlichen transformierenden Wachstumsfaktor beta (TGF-b) bindet, zur Behandlung von soliden Tumoren. Das Unternehmen wurde im Jahr 2018 gegründet und hat seinen Sitz in Boston, Massachusetts. Bicara Therapeutics Inc. ist eine Tochtergesellschaft von Biocon Limited.

Nombre
Bicara Therapeutics
CEO
Claire Mazumdar Clemon
Sede Boston, ma
Estados Unidos
Sitio web
Industria
Productos químicos
Salida a bolsa
13/09/2024
Empleados 103

Símbolos bursátiles

Bolsa Símbolo
NASDAQ
BCAX
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