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Il prezzo obiettivo medio degli analisti è 5,18 € (+3884,62%). La mediana è 5,18 € (+3884,62%).
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China approves CASI Pharmaceuticals phase‑1/2 study for CID‑103 against antibody‑mediated kidney transplant rejection
China's NMPA has approved a clinical phase‑1/2 trial application for CASI Pharmaceuticals' monoclonal anti‑CD38 antibody CID‑103 to treat chronic active antibody‑mediated rejection (AMR) after kidney transplantation. The study will evaluate tolerability, safety and efficacy in AMR patients; the FDA had previously granted an IND for a phase‑1 trial. CASI, which holds worldwide rights to CID‑103, calls the drug a potential best‑in‑class therapy; the announcement was accompanied by a roughly 20% rise in the company's share price. » Altro su de.investing.com
CASI Pharmaceuticals receives extension for Nasdaq listing deadline until February 17, 2026
The Nasdaq Hearings Panel granted CASI Pharmaceuticals an extension to restore the minimum $35 million market capitalization required under Rule 5550(b)(2); trading remains suspended until the requirements are met. The market capitalization currently stands at only $15.47 million and the stock is trading near its 52-week low. CASI also secured $20 million in financing through convertible notes, reported positive interim results from the Phase 1 study of CID-103, and obtained FDA clearance for a Phase 1 study in antibody-mediated kidney rejection with the first patient expected to be treated in Q1 2026. Analysts forecast 2025 EPS of $0.54 and a projected revenue decline of 53%. » Altro su de.investing.com
CASI Pharmaceuticals reports positive phase 1 data for CID-103 in ITP
CASI Pharmaceuticals reports interim results from an open-label phase 1 study of CID-103 in immune thrombocytopenia (ITP): 8 of 11 patients (73%) met the primary efficacy endpoint, 6 of the 8 showed a complete response, and platelet improvements appeared as early as one week. CID-103 had a manageable safety profile with two treatment-related grade 3 events and no dose-limiting toxicities. The study is running across five dose cohorts; pharmacodynamic markers decreased consistently with the mechanism of action. On the financial side, the small-cap company has a current ratio of 0.3, is trading near its 52-week low, and received a delisting notice from NASDAQ for falling below the minimum market value requirement. » Altro su de.investing.com
Dati finanziari dell'azienda
| (EUR) | set 2025 | |
|---|---|---|
| Ricavi | 2,62 Mln | - |
| Utile lordo | 601,6K | - |
| Utile netto | -9,27 Mln | - |
| EBITDA | -8,61 Mln | - |
Dati fondamentali
| Metrica | Valore |
|---|---|
Capitalizzazione di mercato | 2,01 Mln € |
Numero di azioni | 15,49 Mln |
Massimo/minimo a 52 settimane | 2,67 € - 0,12 € |
| Dividendi | No |
Beta | 0,89 |
Rapporto P/E | -0,05 |
Rapporto PEG | 0,01 |
Rapporto P/B | -0,08 |
Rapporto P/S | 0,14 |
Profilo aziendale
CASI Pharmaceuticals, Inc. ist ein biopharmazeutisches Unternehmen, das Therapeutika und pharmazeutische Produkte in China, den Vereinigten Staaten und international entwickelt und vertreibt. Es bietet EVOMELA an, eine intravenöse Formulierung von Melphalan zur Verwendung als Konditionierungstherapie vor einer Stammzelltransplantation und als palliative Behandlung für Patienten mit multiplem Myelom. Die Produktpipeline des Unternehmens umfasst CNCT19, ein autologes CD19-CAR-T-Prüfpräparat für die Behandlung von Patienten mit akuter B-Zell-Lymphoblastenleukämie (B-ALL) und B-Zell-Non-Hodgkin-Lymphom (B-NHL); BI-1206, das sich in einer Phase-I/II-Studie in Kombination mit der Anti-PD1-Therapie Keytruda bei soliden Tumoren und in einer Phase-I/IIa-Studie in Kombination mit MabThera (Rituximab) bei Patienten mit rezidiviertem/refraktärem NHL befindet; und CB-5339, das sich in einer klinischen Phase-I-Studie für akute myeloische Leukämie und myelodysplastisches Syndrom befindet. Die Produktpipeline des Unternehmens umfasst außerdem CID-103 für die Behandlung von Patienten mit multiplem Myelom, Thiotepa, das mehrere Indikationen hat, darunter die Verwendung als Konditionierungstherapie für verschiedene allogene hämatopoetische Stammzelltransplantationen, und Octreotid in langwirksamen injizierbaren Formulierungen für die Behandlung von Akromegalie und für die Kontrolle von Symptomen im Zusammenhang mit verschiedenen neuroendokrinen Tumoren. Das Unternehmen hat Lizenzvereinbarungen mit Juventas Cell Therapy Ltd, BioInvent International AB, Black Belt Therapeutics Limited und Cleave Therapeutics, Inc. Es hat auch Vertriebsvereinbarungen mit China Resources Pharmaceutical Commercial Group International Trading Co., Ltd; Pharmathen Global BV; und Riemser Pharma GmbH. Das Unternehmen war früher als EntreMed, Inc. bekannt und änderte im Juni 2014 seinen Namen in CASI Pharmaceuticals, Inc. CASI Pharmaceuticals, Inc. wurde 1991 gegründet und hat seinen Sitz in Rockville, Maryland.
| Nome | CASI Pharmaceuticals |
| CEO | David A. Cory |
| Sede centrale | Beijing,
md Stati Uniti |
| Sito web | |
| Settore | Beni di prima necessità |
| Industria | Prodotti alimentari |
| Quotazione in borsa | 12/06/1996 |
| Dipendenti | 233 |
Simboli di borsa
| Borsa | Simbolo |
|---|---|
NASDAQ | CASI |
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