Informationstyper: PRM
The last patient visit was completed in Stayble Therapeutics’ herniated disc study
Stayble Therapeutics AB (“Stayble” or “the Company”) announced today that the last patient visit has been completed in the phase 1b study involving patients with pain caused by herniated discs. This company follows the previously communicated timeline and expects to present results during the fourth quarter of 2024.
Stayble receives its first approved patent for the treatment of herniated discs
Stayble Therapeutics AB (“Stayble” or “the Company”) announced today that the South African patent office, as the first country, has approved the Company’s patent for the treatment of herniated discs with STA363. This approval is a significant milestone for the Company and follows a previous positive international search report from European authorities. With these advancements, we see strong potential to obtain several additional national patent approvals.
Stayble Therapeutics publishes half-year report for 2024
Stayble Therapeutics AB (“Stayble” or the “Company”) hereby publishes its half-year report for 2024. The report is available as an attached document and on the Company’s website: https://staybletherapeutics.com/investor-relations/financial-reports/. Below is a summary of the report.
Stayble Therapeutics appoints new CFO
Stayble Therapeutics AB announces that Erik Kullgren has been appointed as the new CFO, effective August 1, 2024.
Stayble Therapeutics presents positive interim data from the ongoing phase Ib study with STA363
Stayble Therapeutics AB (“Stayble” or the “Company”) announces today that the Company’s phase Ib study has reached the follow-up goal of at least 18 patients completing their three-month visit. A total of 24 patients completed the visit. All essential data for evaluating the study’s primary parameters have thus been secured. The company also presents positive interim data with established safety and tolerability (primary study objective) when evaluating available blinded data from the three-month follow-up. The patients will be followed until they complete their six-month visit. Then, the study is unblinded, and patients are divided into groups of those treated with STA363 or placebo. Today, approximately half of the patients have completed their six-month visit. The study is proceeding fully as planned, and the final results are expected to be presented in Q4 2024.
(SV) Stayble Therapeutics AB (publ) offentliggör utfall i riktad emission av units
EJ FÖR PUBLICERING, DISTRIBUTION ELLER OFFENTLIGGÖRANDE, DIREKT ELLER INDIREKT, HELT ELLER DELVIS, INOM ELLER TILL USA, AUSTRALIEN, HONGKONG, JAPAN, KANADA, NYA ZEELAND, SCHWEIZ, SINGAPORE, SYDAFRIKA, SYDKOREA, RYSSLAND, BELARUS ELLER NÅGON ANNAN JURISDIKTION DÄR SÅDAN PUBLICERING, DISTRIBUTION ELLER OFFENTLIGGÖRANDE SKULLE VARA I STRID MED GÄLLANDE REGLER ELLER KRÄVA YTTERLIGARE REGISTRERING ELLER ANDRA ÅTGÄRDER ÄN VAD SOM FÖLJER AV SVENSK RÄTT. DETTA PRESSMEDDELANDE UTGÖR INTE ETT ERBJUDANDE ATT FÖRVÄRVA VÄRDEPAPPER I STAYBLE THERAPEUTICS AB (PUBL). SE ÄVEN AVSNITTET ”VIKTIG INFORMATION” NEDAN.
Stayble Therapeutics AB (publ) (”Stayble” eller ”Bolaget”) meddelar utfallet i den riktade emission av units till vissa externa investerare (Fredrik Åhlander, Gerhard Dal, Jens Miöen, Jens Olsson, Jinderman & Partners AB (https://jinderman.se), John Moll, Niklas Estensson, Nils Berg och Stefan Hansson), dels den befintliga aktieägaren Chalmers Ventures AB som styrelsen den 11 juni 2024 beslutat om med stöd av emissionsbemyndigande (den ”Riktade Emissionen”). Samtliga 4 000 000 units, motsvarande totalt 12 000 000 aktier och 8 000 000 teckningsoptioner av serie TO2, tecknades och styrelsen i Bolaget har därför beslutat om tilldelning av samtliga units i den Riktade Emissionen.
(SV) Stayble Therapeutics AB (publ) genomför en riktad emission av units om totalt cirka tre miljoner kronor inför kommande resultat från fas 1b-studien
EJ FÖR PUBLICERING, DISTRIBUTION ELLER OFFENTLIGGÖRANDE, DIREKT ELLER INDIREKT, HELT ELLER DELVIS, INOM ELLER TILL USA, AUSTRALIEN, HONGKONG, JAPAN, KANADA, NYA ZEELAND, SCHWEIZ, SINGAPORE, SYDAFRIKA, SYDKOREA, RYSSLAND, BELARUS ELLER NÅGON ANNAN JURISDIKTION DÄR SÅDAN PUBLICERING, DISTRIBUTION ELLER OFFENTLIGGÖRANDE SKULLE VARA I STRID MED GÄLLANDE REGLER ELLER KRÄVA YTTERLIGARE REGISTRERING ELLER ANDRA ÅTGÄRDER ÄN VAD SOM FÖLJER AV SVENSK RÄTT. DETTA PRESSMEDDELANDE UTGÖR INTE ETT ERBJUDANDE ATT FÖRVÄRVA VÄRDEPAPPER I STAYBLE THERAPEUTICS AB (PUBL). SE ÄVEN AVSNITTET ”VIKTIG INFORMATION” NEDAN.
Stayble Therapeutics AB (publ) (”Stayble” eller ”Bolaget”) genomför en riktad emission av sammanlagt 4 000 000 units, där varje unit består av tre (3) nyemitterade aktier och två (2) teckningsoptioner av serie TO2 i Bolaget, motsvarande totalt 12 000 000 aktier och 8 000 000 teckningsoptioner av serie TO2 (den ”Riktade Emissionen”). De teckningsberättigade i den Riktade Emissionen är dels ett antal externa investerare (Fredrik Åhlander, Gerhard Dal, Jens Miöen, Jens Olsson, Jinderman & Partners AB (https://jinderman.se), John Moll, Niklas Estensson, Nils Berg och Stefan Hansson), dels den befintliga aktieägaren Chalmers Ventures AB. Beslut om den Riktade Emissionen har fattats av styrelsen med stöd av emissionsbemyndigande. Teckningskursen har fastställts genom förhandlingar med investerarna på armlängds avstånd och uppgår till 0,75 kronor per unit, motsvarande 0,25 kronor per aktie. Teckningsoptionerna emitteras vederlagsfritt. Teckningsåtaganden har ingåtts avseende den totala emissionsvolymen. Genom den Riktade Emissionen tillförs Bolaget därmed initialt cirka tre (3) miljoner kronor före avdrag för transaktionskostnader, och för det fall samtliga vidhängande teckningsoptioner av serie TO2 nyttjas för teckning av aktier i Bolaget kommer Bolaget att, beroende på teckningskursen vid utnyttjande av teckningsoptionerna, tillföras ytterligare cirka två (2) till tre (3) miljoner kronor före avdrag för transaktionskostnader.
Stayble Therapeutics publishes interim report for the first quarter of 2024
Stayble Therapeutics AB (“Stayble” or the “Company”) hereby publishes its interim report for the first quarter of 2024. The report is available as an attached document and on the Company’s website, https://staybletherapeutics.com/investor-relations/financial-reports/. Below is a summary of the report.
(SV) Kommuniké från årsstämman i Stayble Therapeutics
Stayble Therapeutics AB, org.nr 559024-8372 (“Bolaget”), har hållit årsstämma den 15 maj 2024 kl. 13.00 på Bolagets kontor på Lennart Torstenssonsgatan 8 i Göteborg. Vid stämman fattades beslut om, bland annat, nedanstående.
(SV) Stayble Therapeutics publicerar årsredovisningen för 2023
Stayble Therapeutics AB (”Stayble” eller ”Bolaget”) publicerar idag årsredovisningen för 2023. Årsredovisningen finns tillgänglig på bolagets hemsida (https://staybletherapeutics.com/sv/investerare/finansiella-rapporter/) och bifogad i detta utskick.
(SV) Kallelse till årsstämma i Stayble Therapeutics AB
Aktieägarna i Stayble Therapeutics AB, org.nr 559024-8372, kallas till årsstämma den 15 maj 2024 kl. 13.00 på bolagets kontor på Lennart Torstenssonsgatan 8 i Göteborg. Inregistrering till årsstämman påbörjas kl. 12.30.
Abstract on STA363’s clinical effect on disc volume has been accepted for presentation at an important congress
Stayble Therapeutics AB (“Stayble” or the “Company”) announces that the Company’s scientific abstract regarding the treatment concept for herniated discs has been accepted for a poster presentation at the International Society for the Study of the Lumbar Spine (ISSLS) annual meeting in Milan, Italy, on 27-31 May 2024.
All patients included in Stayble Therapeutics’ phase Ib study in disc hernia with STA363
Stayble Therapeutics AB (“Stayble” or the “Company”) announces today that the last patient has been included in the ongoing phase Ib clinical study with STA363 towards disc hernia. No significant side effects have so far been reported and currently, none of the included patients has discontinued their participation in the study. Results from the study are expected to be available in Q4 2024.
Stayble Therapeutics publishes year-end report for 2023
Stayble Therapeutics AB (“Stayble” or the “Company”) hereby publishes its year-end report for 2023. The report is available as an attached document and on the Company’s website, https://staybletherapeutics.com/investor-relations/financial-reports/. Below is a summary of the report.
Stayble Therapeutics presents the final data from the phase IIb study
Stayble Therapeutics AB (“Stayble” or the “Company”) today presents the final data analysis of the Company’s phase IIb study with STA363 against chronic disc-related back pain (degenerative disc disease, “DDD”). Consistent with the preliminary topline analysis communicated in a previous press release, the subgroup analyses verify previously announced results where no difference in pain between placebo and active groups could be detected. In patients who received the higher dose of STA363, a statistically significant difference in disc intensity was observed and in both active doses a statistically significant reduction in disc height was shown. These changes clearly show that STA363 affects the disc and produces a reduced disc volume.
Stayble Therapeutics Phase IIb data support effectiveness in treating herniated discs
Stayble Therapeutics AB (“Stayble” or the “Company”) today presents further analyses from the Phase IIb study on degenerative disc disease (DDD) and its impact on the Company’s other project on lumbar disc herniation (LDH). In patients who received the higher dose of STA363, a statistically significant difference was observed in disc intensity and disc height, which are clear signs of reduced disc volume. These effects should lead to a decrease in the volume of the herniation and, thus, pain reduction in patients with herniated discs.
Correction: Stayble Therapeutics publishes interim report for the third quarter of 2023
Republishes with MAR text in the press release. No changes have been made to the press release or the attached report.
Stayble Therapeutics AB (“Stayble” or the “Company”) hereby publishes its quarterly report for the third quarter of 2023. The report is available as an attached document and on the Company’s website, www.staybletherapeutics.com/en/investors/financial-reports/. Below is a summary of the report.
Stayble Therapeutics publishes interim report for the third quarter of 2023
Stayble Therapeutics AB (“Stayble” or the “Company”) hereby publishes its quarterly report for the third quarter of 2023. The report is available as an attached document and on the Company’s website, www.staybletherapeutics.com/en/investors/financial-reports/. Below is a summary of the report.
Stayble Therapeutics reports top-line data from the company’s phase IIb study
Stayble Therapeutics AB (“Stayble” or the “Company”) today presents top-line data from the Company’s phase IIb study with STA363 for the treatment of degenerative disc disease, “DDD”. The randomized, double-blind study did not meet the primary objective. According to the pre-specified statistical criteria, STA363 compared to placebo did not show a statistically significant reduction in pain at six months.
Stayble Therapeutics engages Ferghana Partners to support partnering activities
Stayble Therapeutics AB (“Stayble” or the “Company”) today announces that it has entered into an agreement with the transaction advisor Ferghana Partners (“Ferghana”) ahead of the upcoming clinical results from the STA363 phase 2b study in patients with chronic back pain caused by degenerative disc disease. Provided results are positive, Ferghana will assist Stayble with international partnering activities for STA363, accelerate such activities, and supplement Stayble’s current resources.