Xintela signs with Australian CRO for clinical study

Xintela announces today that the company has signed a contract with GreenLight Clinical, an Australian Contract Research Organisation (CRO) to conduct Xintela's First-in-Human study using the stem cell product XSTEM.

Xintela's First-in-Human study with the stem cell product XSTEM, a combined phase I/II clinical study on patients with knee osteoarthritis, will be conducted in Australia and is planned to be initiated in Q4 2021. An agreement with the Contract Research Organisation (CRO) GreenLight Clinical (GLC), headquartered in Sydney, Australia, has now been signed. Xintela has collaborated with GLC since 2019, and this now continues with the full-service execution of the clinical study.

"We are very pleased to have selected GreenLight Clinical (GLC) as our partner in this First-In-Human study. We have for some time worked with GLC on regulatory matters and preparation of core clinical documents. We have established a productive working relationship and good foundation to continue our partnership as Xintela now enters clinical development of XSTEM. At the same time, Xintela is strengthening our clinical development team in-house, which is essential to successfully drive our clinical programs forward", says Xintela's CEO, Evy Lundgren-Åkerlund.

"We are delighted to partner with Xintela for the XSTEM-OA study, and further strengthen the close ties between our respective organizations. GreenLight and Xintela share a common goal of bringing new and innovative treatments to patients in need. With Australia's renowned clinical research environment, GreenLight's personal and customised approach will enable Xintela to rapidly advance the XSTEM program. We look forward to working closely once again with Xintela, and take this product into the clinic, and beyond", says GreenLight Clinical's CEO, Franz D'Lima.

Xintela AB (publ)
Evy Lundgren-Åkerlund, CEO
Tel: +46 46 275 65 00
Email: [email protected]
Medicon Village
223 81 Lund, Sweden
www.xintela.se

About GreenLight Clinical
GreenLight Clinical is a full-service CRO specialised in early phase studies, based in Australia with operations across North America, Europe and Asia Pacific. For more information, please refer to www.greenlightclinical.com.

About Xintela
Xintela develops innovative and patent protected cell therapies and targeted cancer therapies based on the marker technology platform XINMARK. The platform is built on specific cell surface proteins (integrins) and more than 25 years of research and development. Xintela uses the marker technology to select and quality assure stem cells (XSTEM) to develop stem cell therapies for diseases that today lack efficient treatment options, including the joint disease osteoarthritis (OA). Xintela has built an in-house GMP-facility for manufacturing of stem cell products and is preparing a First in Human clinical study on patients with knee OA. In the oncology program, Xintela develops antibody-based therapies for treatment of aggressive tumors including glioblastoma and triple-negative breast cancer. Xintela is listed on Nasdaq First North Growth Market Stockholm since 22 March 2016. Xintela's Certified Adviser at Nasdaq First North Growth Market is Erik Penser Bank AB, +46 8-463 80 00, [email protected]

Targinta väljer läkemedelskandidat för trippelnegativ bröstcancer

Det prekliniska onkologibolaget Targinta har valt sin första läkemedelskandidat, TARG10, en terapeutisk antikropp riktad mot målproteinet integrin a10b1. TARG10 har visat kraftfulla effekter både på cancerceller och i prekliniska tumörmodeller, med minskad tumörtillväxt och minskad metastasering i trippelnegativ bröstcancer.


Targinta selects lead drug candidate for triple-negative breast cancer

The preclinical stage oncology biotech company Targinta has selected its first lead drug candidate, TARG10, a therapeutic antibody targeting integrin a10b1. TARG10 has shown strong activity on cancer cells and in preclinical tumor models, with significant inhibitory effects on both growth and metastasis in triple-negative breast cancer models.


Xintela breddar klinisk utveckling av stamcellsprodukten XSTEM

Lund, Sverige, 30 september 2021 - Xintela meddelar att bolaget utökar det kliniska utvecklingsarbetet av sin stamcellsprodukt XSTEM till nästa valda indikation, venösa bensår, den vanligaste formen av svårläkta (kroniska) sår hos människor. Ett vetenskapligt rådgivningsmöte med Läkemedelsverket har framgångsrikt genomförts och arbetet med att ta fram dokumentation för en ansökan om klinisk studie på venösa bensår har initierats.


Xintela to expand clinical development of stem cell product XSTEM

Lund, Sweden, September 30 2021 - Xintela announces it will expand clinical development of its stem cell product XSTEM to the next chosen indication venous leg ulcers, the most common type of difficult-to-heal (chronic) wounds in humans. A scientific advice meeting with the Swedish Medical Products Agency (MPA) has been successfully completed and preparation of clinical documentation for the clinical study application has been initiated.




Xintela tecknar avtal med australiensisk CRO för klinisk studie

Xintela meddelar idag att företaget har tecknat ett avtal med GreenLight Clinical, en australiensisk CRO (Contract Research Organization) för att genomföra Xintelas första kliniska studie i människa med stamcellsprodukten XSTEM.


Xintela signs with Australian CRO for clinical study

Xintela announces today that the company has signed a contract with GreenLight Clinical, an Australian Contract Research Organisation (CRO) to conduct Xintela's First-in-Human study using the stem cell product XSTEM.


Kommuniké från extra bolagsstämma i Xintela

Xintela 5 juli 2021 - Idag hölls en extra bolagsstämma i Xintela AB. Nedan följer en sammanfattning av de beslut som fattades. Samtliga beslut fattades med erforderlig majoritet.


Xintela bildar dotterbolag i Australien

Xintela har bildat ett helägt dotterbolag, Xindu Pty Ltd, i Australien som ska administrera bolagets kommande kliniska studie på artrospatienter.


Xintela incorporates subsidiary in Australia

Xintela has formed a wholly owned subsidiary, Xindu Pty Ltd, in Australia, which will administer the company's upcoming clinical study on osteoarthritis patients.


Kallelse till extra bolagsstämma i Xintela AB

Aktieägarna i Xintela AB, org.nr 556780-3480, ("Bolaget") kallas härmed till extra bolagsstämma måndag den 5 juli 2021.


Xintela har genomfört en riktad nyemission av aktier och tillförs därigenom cirka 28 MSEK

Lund, 2021-06-17

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 ELLER NÅGON ANNAN JURISDIKTION DÄR SÅDAN PUBLICERING, DISTRIBUTION ELLER OFFENTLIGGÖRANDE SKULLE VARA I STRID MED GÄLLANDE REGLER ELLER KRÄVA YTTERLIGARE REGISTRERING ELLER ANDRA ÅTGÄRDER.

INSIDERINFORMATION: Xintela AB (publ) ("Xintela" eller "Bolaget") har, i enlighet med vad som offentliggjordes i Bolagets pressmeddelande igår, framgångsrikt genomfört en riktad kontant nyemission om 11 965 812 aktier till en teckningskurs om 2,34 SEK per aktie (den "Riktade Emissionen"). Genom den Riktade Emissionen tillförs Bolaget cirka 28 MSEK före avdrag för kostnader relaterade till den Riktade Emissionen. Teckningskursen i den Riktade Emissionen fastställdes genom ett accelererat bookbuilding-förfarande som genomförts av Vator Securities. Investerarna i den Riktade Emissionen utgörs av ett antal svenska och internationella professionella investerare. Därutöver har Maarten de Chateau, styrelseledamot i Xintela, tecknat aktier motsvarandes cirka 3 MSEK i den Riktade Emissionen.


Xintela has completed a directed new share issue raising proceeds of approximately SEK 28 million

Lund, 2021-06-17

NOT FOR RELEASE, DISTRIBUTION OR PUBLICATION, FULLY OR PARTLY, DIRECTLY OR INDIRECTLY, IN THE UNITED STATES OF AMERICA, AUSTRALIA, HONG KONG, CANADA, JAPAN, NEW ZEALAND, SWITZERLAND, SOUTH AFRICA, SOUTH KOREA, OR ANY OTHER JURISDICTION IN WHICH THE RELEASE, DISTRIBUTION OR PUBLICATION WOULD BE UNLAWFUL OR REQUIRE REGISTRATION OR ANY OTHER MEASURE IN ACCORDANCE WITH APPLICABLE LAW.

INSIDE INFORMATION: Xintela AB (publ) ("Xintela" or the "Company") has, in accordance with the Company's press release yesterday, resolved to issue 11,965,812 new shares at a subscription price of SEK 2.34 (the "Directed Issue"). The Company will receive approximately SEK 28 million through the Directed Issue before deductions for costs related to the Directed Issue. The subscription price in the Directed Issue was determined through an accelerated bookbuilding procedure conducted by Vator Securities. The investors in the Directed Issue consist of a number of Swedish and international professional investors. In addition, Maarten de Chateau, a board member of Xintela, has subscribed for shares corresponding to approximately SEK 3 million in the Directed Issue.


Xintela intends to carry out a directed share issue through an accelerated book building procedure

Lund, 2021-06-16

NOT FOR RELEASE, DISTRIBUTION OR PUBLICATION, FULLY OR PARTLY, DIRECTLY OR INDIRECTLY, IN THE UNITED STATES OF AMERICA, AUSTRALIA, HONG KONG, CANADA, JAPAN, NEW ZEALAND, SWITZERLAND, SOUTH AFRICA, SOUTH KOREA, OR ANY OTHER JURISDICTION IN WHICH THE RELEASE, DISTRIBUTION OR PUBLICATION WOULD BE UNLAWFUL OR REQUIRE REGISTRATION OR ANY OTHER MEASURE IN ACCORDANCE WITH APPLICABLE LAW.

INSIDE INFORMATION: Xintela AB (publ) ("Xintela" or the "Company") hereby announces the Company's intention to carry out a new share issue, with deviation from the shareholders' preferential rights of approximately SEK 25 million, with an option to upsize the new share issue, through an accelerated bookbuilding procedure (the "Directed Issue"). The purpose of the Directed Issue is to finance the start of a clinical phase I/IIa study for stem cell treatment of knee osteoarthritis and within Oncology continue preclinical studies of the Company's targeted antibodies for the treatment of glioblastoma and triple negative breast cancer. The Directed Issue is intended to be carried out based on the authorization from the Annual General Meeting on 7 May 2021. The Directed Issue will be offered to professional investors. The Company has mandated Vator Securities to investigate the conditions for carrying out the Directed Issue.


Xintela avser att genomföra en riktad nyemission av aktier genom ett accelererat bookbuilding-förfarande

Lund, 2021-06-16

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 ELLER NÅGON ANNAN JURISDIKTION DÄR SÅDAN PUBLICERING, DISTRIBUTION ELLER OFFENTLIGGÖRANDE SKULLE VARA I STRID MED GÄLLANDE REGLER ELLER KRÄVA YTTERLIGARE REGISTRERING ELLER ANDRA ÅTGÄRDER.

INSIDERINFORMATION: Xintela AB (publ) ("Xintela" eller "Bolaget") offentliggör härmed Bolagets avsikt att genomföra en nyemission, med avvikelse från aktieägarnas företrädesrätt, om cirka 25 MSEK, med möjlighet att utöka nyemissionen, genom ett accelererat bookbuilding-förfarande (den "Riktade Emissionen"). Syftet med den Riktade Emissionen är att finansiera start av en klinisk fas I/IIa studie för stamcellsbehandling av knäartros och inom Onkologi fortsätta prekliniska studier av Bolagets riktade antikroppar för behandling av glioblastom och trippelnegativ bröstcancer. Den Riktade Emissionen avses att genomföras med stöd av bemyndigande från årsstämman den 7 maj 2021. Den Riktade Emissionen kommer att erbjudas till professionella investerare. Bolaget har uppdragit åt Vator Securities att utreda förutsättningarna för att genomföra den Riktade Emissionen.


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