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Prévisions
L'objectif de cours moyen des analystes est de 31,00 € (+62,56 %). La médiane est de 31,22 € (+63,71 %).
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13 |
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0 |
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0 |
Actualités Accéder au fil d'actualités
Immunome bets on ADCs and aims for approval of Varegacestat
At the H.C. Wainwright conference, Immunome presented a two‑pronged strategy: in the short term, securing FDA approval and commercial launch of Varegacestat for desmoid tumors (PDUFA date set); and in the long term, building a broad ADC portfolio. The lead program is the ROR1‑targeted ADC IM‑1021, with the goal of achieving breakthrough designation through strong efficacy. The company highlights its HC74‑Topo1 payload platform and plans to develop at least 10 novel ADCs, but discloses no financial figures and points to the typical risks of early drug development. » Plus sur de.investing.com
Immunome treats first patient in phase 1 study of IM-3050
Immunome has treated the first patient in an open-label, multicenter phase 1 study of the radioligand therapy IM-3050, which delivers radioactive lutetium-177 selectively to FAP-expressing cells in advanced solid tumors. The study is evaluating safety, tolerability, dosimetry, pharmacokinetics and preliminary antitumor activity and includes a dose-escalation to determine the maximum tolerated dose followed by an expansion phase. Immunome notes a clinical pipeline with additional agents and a submitted regulatory application for Varegacestat; analysts have recently raised their earnings estimates and set price targets between $30 and $40. » Plus sur de.investing.com
Immunome: FDA accepts NDA for varegacestat in desmoid tumors
The FDA has accepted the New Drug Application (NDA) for varegacestat, an oral gamma-secretase inhibitor for the treatment of desmoid tumors in adults, and set the PDUFA date for April 28, 2027. The application is supported by the Phase 3 RINGSIDE study (156 patients), which met its primary endpoint and showed an 84% reduction in the risk of disease progression or death versus placebo (HR 0.16; p<0.0001); secondary endpoints and the objective response rate (56% vs. 9%) were also significantly better. The most common adverse events were diarrhea, fatigue, rash, nausea and cough, mostly grade 1–2. Immunome plans an EMA filing by the end of 2026; the company has a market capitalization of $2.76 billion and more cash than debt. » Plus sur de.investing.com
Données financières de l'entreprise
| (EUR) | juin 2026 | |
|---|---|---|
| Chiffre d'affaires | 0 | 100,00 % |
| Bénéfice brut | 0 | 100,00 % |
| Bénéfice net | -64,07 M | 74,03 % |
| EBITDA | -63,24 M | 74,65 % |
Données fondamentales
| Indicateur | Valeur |
|---|---|
Capitalisation boursière | 1,8 Md € |
Nombre d'actions | 95,6 M |
Plus haut/bas sur 52 semaines | 26,44 € - 9,75 € |
| Dividendes | Non |
Bêta | 2,13 |
Ratio P/E | -8,43 |
Ratio PEG | -0,50 |
Ratio P/B | 4,62 |
Ratio P/S | 0,00 |
Profil de l'entreprise
Immunome, Inc. ist ein biopharmazeutisches Unternehmen, das Antikörpertherapeutika für die Onkologie und Infektionskrankheiten entdeckt und entwickelt. Das führende Onkologieprogramm des Unternehmens umfasst IMM-ONC-01, das auf den vom Tumor stammenden Immun-Checkpoint IL-38 abzielt, der die Umgehung des Immunsystems fördert. Außerdem entwickelt es IMM-BCP-01, einen Antikörper-Cocktail-Produktkandidaten für die Behandlung von SARS-CoV-2-Infektionen und COVID-19. Das Unternehmen wurde im Jahr 2006 gegründet und hat seinen Hauptsitz in Exton, Pennsylvania.
| Nom | IMMUNOME INC. DL -,0001 |
| PDG | Clay Siegall |
| Siège social | Bothell,
wa États-Unis |
| Site web | |
| Secteur | Matériaux |
| Industrie | Produits chimiques |
| Introduction en bourse | 02/10/2020 |
| Employés | 247 |
Symboles boursiers
| Bourse | Symbole |
|---|---|
NASDAQ | IMNM |