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Previsión
El precio objetivo medio de los analistas es de 12,95 € (+961,48 %). La mediana es de 12,95 € (+961,48 %).
| Comprar |
3 |
| Mantener |
1 |
| Vender |
0 |
Noticias Ir al feed de noticias
FDA grants Enlivex RMAT status for Allocetra knee osteoarthritis therapy
The FDA has granted Allocetra from Enlivex RMAT designation for the treatment of symptomatic, age-related knee osteoarthritis in patients aged 64 and older. The designation is intended to enable faster and earlier engagement with the agency and may open accelerated review and approval pathways. Enlivex is currently running a randomized Phase IIb study with 182 patients in the US and Europe; the first US patient has already been treated and initial results are expected by the end of Q2 2027. The FDA has also requested a Type B meeting to discuss further development and approval planning; earlier Phase I/IIa data showed significant improvements versus placebo lasting at least six months. » Más en de.investing.com
Enlivex receives NASDAQ deficiency notice for falling below minimum bid price
Enlivex has received a deficiency notice from NASDAQ because its common stock traded below the minimum requirement of $1.00 for 30 consecutive trading days. The stock is currently at $0.72; Enlivex has until November 9, 2026 (180 days) to regain compliance by having a closing bid of at least $1.00 for at least ten consecutive trading days. The company may request an additional 180-day grace period under certain conditions, for example if other listing requirements are met; otherwise a delisting process could follow. The notification has no immediate effect on the listing or trading. » Más en de.investing.com
Enlivex receives approval for phase‑2b study of Allocetra in knee osteoarthritis in Denmark
Enlivex has received approval from the Danish Medicines Agency to enroll patients in the global, multicenter phase‑2b study of Allocetra for moderate to severe age‑related primary knee osteoarthritis. The randomized, double‑blind, placebo‑controlled trial will evaluate the efficacy and safety of intra‑articular Allocetra injections at sites in the US, Denmark and Poland; the FDA had previously approved the US study. Key endpoints are changes in pain and function at three and six months after treatment, as well as quality of life and mobility. According to the company, Enlivex has a strong liquidity position and an exceptional current ratio; however, the stock shows high volatility with a beta of 1.68. » Más en de.investing.com
Datos financieros de la empresa
| (EUR) | dic 2025 | |
|---|---|---|
| Ingresos | 0 | - |
| Beneficio bruto | -64,78 mil | - |
| Beneficio neto | 1059,48 M | - |
| EBITDA | -4,93 M | - |
Datos fundamentales
| Métrica | Valor |
|---|---|
Capitalización bursátil | 21,21 M € |
Número de acciones | 16,83 M |
Máximo/mínimo de 52 semanas | 23,44 € - 1,20 € |
| Dividendos | No |
Beta | 1,47 |
Ratio P/E | 0,00 |
Ratio PEG | 0,00 |
Ratio P/B | 0,00 |
Ratio P/S | 0,00 |
Perfil de la empresa
Enlivex Therapeutics Ltd. ist ein im klinischen Stadium befindliches Unternehmen für Makrophagen-Reprogrammierung und Immuntherapie. Das Unternehmen entwickelt Allocetra, eine zellbasierte Therapie zur Behandlung von Organdysfunktion und -versagen im Zusammenhang mit Sepsis, die sich in einer klinischen Studie der Phase II befindet, sowie eine präklinische Studie zur Behandlung solider Tumore. Enlivex Therapeutics Ltd. wurde 2005 gegründet und hat seinen Hauptsitz in Nes Ziona, Israel.
| Nombre | Enlivex Therapeutics |
| CEO | Oren Hershkovitz |
| Sede | Ness Ziona,
ta Israel |
| Sitio web | |
| Sector | Materiales |
| Industria | Productos químicos |
| Salida a bolsa | 31/07/2014 |
| Empleados | 34 |
Símbolos bursátiles
| Bolsa | Símbolo |
|---|---|
Tlv | ENLV.TA |
NASDAQ | ENLV |
Frankfurt | 1BT.F |
Descubrir activos
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