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LandNorge
ListaOB Match
SektorHälsovård
IndustriBioteknik
BerGenBio är ett norskt onkologibolag. Idag bedriver bolaget forskning och utveckling av hämmande läkemedel för behandling av aggressiva cancertyper. Bolaget har utvecklat ett flertal produkter vars sammansättning ämnar blockera proteinet AXL, ett protein positivt relaterat med spridning av cancercellerna. Bolaget grundades under 2007 och har sitt huvudkontor i Bergen, Norge.
2022-04-26 07:00:05
Complete data analysis confirms that the primary endpoint of improved clinical
response and key secondary endpoints were met in a subprotocol under the
platform ACCORD2 study where bemcentinib was added to standard of care therapy

BerGenBio to confirm the ACCORD2 data by progressing bemcentinib into EU
-SolidAct, a pan-European platform COVID-19 study enrolling up to 500 patients

Bergen, Norway,April 26, 2022 - BerGenBio ASA (OSE:BGBIO), a clinical-stage
biopharmaceutical company developing novel, selective AXL inhibitors for severe
unmet medical needs, announced today that a complete data analysis of a
randomized phase II study of bemcentinib in combination with standard of care
(SoC) therapy, ACCORD2 (BGBIL019), in hospitalized COVID-19 patients confirms
that the primary efficacy endpoint was met.

At the July 2021 European Congress of Clinical Microbiology & Infectious
Diseases (ECCMID) meeting, the Company previously presented preliminary data
from the ACCORD2 study in combination with a second COVID-19 study (BGBC020)
showing evidence of therapeutic benefit on meaningful clinical endpoints in a
total of 177 patients.  Today's announcement is the first time complete ACCORD2
data in a total of 61 treated patients has been separately reported.

Overall, 90% of patients treated with bemcentinib + SoC (26 of 29) experienced a
clinical response by day 29 (median 7.0 days), as defined by either a two-point
improvement in World Health Organization (WHO) category from baseline score, or
discharge from hospital, whichever arose sooner. This compared to 69% (22 of 32
patients) with a clinical response to SoC treatment alone (median 9.5 days),
showing statistical significance.

The data was generated under a sub-protocol of the platform ACCORD2 study
(ACCORD2