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Prognose
Analytikernes gennemsnitlige kursmål er 7,35 € (+245,07 %). Medianen er 7,13 € (+234,74 %).
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Nyheder Til nyhedsfeedet
Adagene partners with Incyte to test muzastotug–INCA33890 combo in MSS colorectal cancer
Adagene will provide muzastotug (ADG126) for a Phase 1 combination trial with Incyte’s INCA33890 targeting MSS colorectal cancer, planned to start in 2026 and focusing on third-line patients with and without liver metastases. Incyte will sponsor and run the study while Adagene supplies the clinical material. The collaboration expands muzastotug’s clinical program after prior combination data showed a 31% overall response rate in certain high-dose cohorts and a median overall survival of 19.8 months in 10 mg/kg cohorts when combined with pembrolizumab. » Mere på finance.yahoo.com
Adagene prices offering of around $70.0 million at $3.75 per ADS
Adagene has priced a guaranteed public offering of 18,666,000 ADS at $3.75 per ADS, implying gross proceeds of approximately $70.0 million. Each ADS represents 1.25 common shares; the offering price is below the current market price and equals the volume-weighted 30-day average. Closing is expected on April 6, 2026; Leerink Partners and LifeSci Capital are joint bookrunners. Investors include both new and existing funds; the company remains unprofitable despite cash on hand and is currently rated overvalued by InvestingPro. » Mere på de.investing.com
Adagene reports 31% response rate in phase‑1b/2 study of Muzastotug in colorectal cancer
Adagene released updated data from its phase‑1b/2 study of Muzastotug plus pembrolizumab in microsatellite‑stable colorectal cancer without liver metastases: in the combined 20 mg/kg cohorts a confirmed overall response rate of 31% was achieved versus 13% in the 10 mg/kg cohorts (data set: 67 patients). Median progression‑free survival was 6.7 months (20 mg/kg) versus 4.8 months (10 mg/kg); the one‑year survival rate was 80.8% and 70.1%, respectively. Safety data showed a discontinuation rate of 4%, no dose‑limiting toxicities and no treatment‑related grade‑4/5 events; grade‑3 adverse events occurred in 15% (10 mg/kg) and 38% (20 mg/kg). The FDA has granted Muzastotug plus pembrolizumab fast‑track status; a randomized phase‑2 trial is recruiting and results are expected in H1 2027. Despite the progress, Adagene remains unprofitable with a market capitalization of $217m, and the stock rose sharply last year. » Mere på de.investing.com
Historisk udbytte Udbytte
Alle nøgletal for udbytte Alle nøgletalVirksomhedstal
| (EUR) | juni 2026 | YoY |
|---|---|---|
| Omsætning | 1,42 mio. | - |
| Bruttofortjeneste | 1,2 mio. | - |
| Nettoresultat | -14,38 mio. | - |
| EBITDA | -14,34 mio. | - |
Fundamentale data
| Nøgletal | Værdi |
|---|---|
Markedsværdi | 81,85 mio. € |
Antal aktier | 37,65 mio. |
Højeste/laveste i 52 uger | 4,32 € - 1,16 € |
| Udbytte | Nej |
Beta | 0,54 |
P/E (PE Ratio) | -5,17 |
PEG (PEG Ratio) | -0,05 |
K/I (PB Ratio) | 1,04 |
P/S (PS Ratio) | 9,86 |
Virksomhedsprofil
Adagene Inc., et klinisk fase virksomhed inden for biofarmaceutiske produkter, beskæftiger sig med forskning, udvikling og produktion af monoklonale antistofmediciner til kræft. Virksomhedens produktkandidater omfatter ADG106, et humant ligand-blokerende agonistisk anti-CD137 monoklonalt antistof (mAb), som er i fase 1b/2 kliniske forsøg til behandling af avancerede solide tumorer og non-Hodgkin-lymfom; ADG126, et fuldt humant anti-CTLA-4 mAb, som er i et fase 1 klinisk forsøg til behandling af avancerede/metastatiske solide tumorer; og ADG116, et humant ligand-blokerende anti-CTLA-4 mAb, som er i et fase I klinisk forsøg til behandling af avancerede metastatiske solide tumorer. Virksomheden tilbyder også ADG104, et anti-PD-L1 mAb, som er i klinisk udvikling i fase 2; ADG125, et nyt anti-CSF-1R mAb, som er i et fase I klinisk forsøg; ADG206, et maskeret, Fc-konstrueret anti-CD137 agonistisk POWERbody, som er i prækliniske studier; ADG153, et maskeret anti-CD47 IgG1 SAFEbody, som er i prækliniske studier til behandling af hæmatologiske og solide tumorer; ADG138, et nyt HER2xCD3 POWERbody, som er i prækliniske studier til behandling af HER2-udtrykkende solide tumorer; og ADG152, et CD20xCD3 POWERbody, som er i prækliniske studier til behandling af off-tumor-toksicitet. Virksomheden blev stiftet i 2011 og har hovedkontor i Suzhou, Kina.
| Navn | Adagene ADR Aktie |
| CEO | Peter Luo |
| Hjemsted | Suzhou,
js Kina |
| Websted | |
| Sektor | Materialer |
| Branche | Kemikalier |
| Børsnotering | 09.02.2021 |
| Medarbejdere | 128 |
Deep Dive
Tickersymboler
| Børs | Symbol |
|---|---|
NASDAQ | ADAG |
Frankfurt | 978.F |
Düsseldorf | 978.DU |
München | 978.MU |