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Tid*
2025-03-31 N/A Bokslutskommuniké 2024
2024-11-08 - Kvartalsrapport 2024-Q3
2024-08-30 - Kvartalsrapport 2024-Q2
2024-06-14 - Årsstämma
2024-06-03 - X-dag ordinarie utdelning BIOSGN 0.00 SEK
2024-05-31 - Kvartalsrapport 2024-Q1
2024-02-29 - Bokslutskommuniké 2023
2023-11-30 - Kvartalsrapport 2023-Q3
2023-08-31 - Kvartalsrapport 2023-Q2
2023-05-31 - Årsstämma
2023-05-31 - Kvartalsrapport 2023-Q1
2023-05-02 - X-dag ordinarie utdelning BIOSGN 0.00 SEK
2023-03-31 - Bokslutskommuniké 2022
2022-11-30 - Kvartalsrapport 2022-Q3
2022-08-31 - Kvartalsrapport 2022-Q2
2022-06-30 - Årsstämma
2022-05-31 - Kvartalsrapport 2022-Q1
2022-04-29 - X-dag ordinarie utdelning BIOSGN 0.00 SEK
2022-03-31 - Bokslutskommuniké 2021
2021-11-30 - Kvartalsrapport 2021-Q3

Beskrivning

LandSverige
ListaFirst North Stockholm
SektorHälsovård
IndustriBioteknik
Biosergen är verksamt inom bioteknik. Bolaget är specialiserat inom forskning och utveckling av diverse läkemedel. Produktportföljen inkluderar exempelvis bolagets produkt BSG005, ett svampdödande läkemedel i klinisk fas. Utöver huvudverksamheten erbjuds även service och tillhörande kringtjänster. Verksamheten bedrivs i Norge. Biosergen grundades år 2004 och har sitt huvudkontor i Solna.
2024-11-26 11:57:15

November 26, 2024 - Biosergen AB ("Biosergen"), a clinical-stage biotechnology company developing therapies for life-threatening fungal infections, is pleased to announce that the first two patients in the second cohort of its ongoing proof-of-concept clinical trial for BSG005 has successfully begun treatment with BSG005. The patients are suffering from a severe infection caused by Aspergillus and Mucor Mycosis respectively. These two patients represent challenging cases where current antifungal treatments have proven ineffective due to resistance and renal impairment.

"It is exciting to advance to this next stage of dosing with BSG005," said Tine Olesen, CEO of Biosergen. "For patients with no effective options, BSG005 has the potential to be lifesaving, especially if the promising safety and efficacy results from the first cohort continue. As we progress through dose escalation, we hope to continue to observe no severe side effects, allowing us to gain deeper insights into BSG005's potential for patients in critical need."

Following positive safety and efficacy results from the first cohort, the trial's independent Data Safety Review Committee approved progression to higher dosing in this second cohort. This phase initiates patient treatment at 0.8 mg/kg per day, with potential escalation up to 1.5 mg/kg depending on patient response and safety.

The second cohort will include up to five patients and is performed in collaboration with Biosergen's partners in India, as with the first cohort. Biosergen aims to develop BSG005 as a new standard for treating invasive fungal infections in patients who are resistant to existing treatments or are ineligible for such treatment due to kidney impairment.