Xintela appoints Sven Kili as Chief Operating Officer

Lund, Sweden, 16 April 2019 - Sven Kili, an Executive Director and the Chief Medical Officer of Xintela, extends his commitment by taking on the Chief Operating Officer (COO) role. Sven Kili is a surgeon and specialist in orthopedics and, through leading positions in pharmaceutical companies including Genzyme, Sanofi, and GSK, has many years' experience in the successful development and commercialization of cell and gene therapy products.

"We are very fortunate that Sven Kili now has the opportunity to increase his engagement with Xintela to 50% and take on the additional role of Chief Operating Officer. We are in a very exciting, active phase, preparing for both GMP production of our stem cell product and the start of clinical studies, and Sven's deep experience in these areas will be of tremendous importance. In addition, with his great international network in cell and gene therapy, he will be key to Xintela's financing and internationalization activities," says Xintela's CEO Evy Lundgren-Åkerlund.

"I look forward to spending more time with the Xintela team and to take on more of the challenges in the company's development. Xintela has great ambition and potential with this technology and we have a very exciting journey ahead of us," says Sven Kili.

2019-04-16

Xintela AB (publ)
Evy Lundgren-Åkerlund, CEO
Tel: 070-329 18 71
Email: evy@xintela.se
Medicon Village
223 81 Lund
www.xintela.se

About Xintela
Xintela develops medical products within regenerative medicine and oncology based on its proprietary marker technology, XINMARK®. Xintela uses the technology to isolate and quality assure stem cells for the treatment of the joint disease osteoarthritis. Studies on horses have shown that the stem cells are safe and that they have a therapeutic effect on the articular cartilage and the underlying bone after an injury. Xintela has recently established its own GMP-facility to produce stem cells for clinical studies. In the oncology program, XINMARK® is used for the development of an antibody-based treatment (Antibody Drug Conjugate, ADC) against specific tumors with first focus on the aggressive brain tumor glioblastoma. Positive preclinical results from cell studies and animal model have shown that the ADC treatment has a targeting and killing effect on specific tumor cells supporting further development of the company's oncology business. Xintela is listed on Nasdaq First North Stockholm since 22 March 2016. Xintela's Certified Adviser at Nasdaq First North is Erik Penser Bank AB, +46 8-463 80 00, certifiedadviser@penser.se.

Nerladdningsbara filer

Kommuniké från Xintelas årsstämma 2021

Lund, Sverige, 7 maj 2021 - Idag hölls årsstämma i Xintela AB (publ). Nedan följer en sammanfattning av de beslut som fattades. Samtliga beslut fattades med erforderlig majoritet.


Targinta rekryterar Per Norlén som VD

Lund, Sverige, den 4 maj 2021 - Xintela meddelar idag att Per Norlén har rekryterats som VD för Xintelas helägda dotterbolag Targinta inom onkologi. Han tillträder 1 september 2021. Per Norlén kommer även ha rollen som Xintelas Chief Medical Officer (CMO/Medicinsk Chef) från 1 juli 2021. Rekryteringen är ett viktigt steg i processen med att knoppa av Targinta som ett fristående bolag.


Targinta recruits Per Norlén as CEO

Lund, Sweden, May 4, 2021 - Xintela announces today that Per Norlén has been recruited as CEO of Xintela's wholly owned oncology subsidiary Targinta. He will start on 1 September 2021. Per Norlén will also have the role of Xintela's Chief Medical Officer (CMO) from 1 July 2021. The recruitment is an important step in the process of spinning out Targinta as an independent company.


Xintela offentliggör årsredovisning för 2020

Lund, Sverige, 16 april 2021 - Xintela AB (publ) meddelar idag att bolaget publicerar årsredovisningen för 2020. Årsredovisningen finns tillgänglig på bolagets hemsida www.xintela.se samt via bifogad PDF.


Inspektion av Xintelas GMP-verksamhet för tillverkningstillstånd genomförd

Lund, Sverige, den 12 april 2021 - Xintela meddelar idag att Läkemedelsverket har genomfört en inspektion för tillstånd att producera cellterapiprodukter, så kallade avancerade terapiläkemedel (ATMPs), för kliniska studier.


Xintela GMP inspection for manufacturing license completed

Lund, Sweden, 12 April 2021 - Xintela announces today completion of the inspection by the Swedish Medical Products Agency for a license to produce cell therapy products, also known as Advanced Therapy Medicinal Products (ATMPs), for clinical studies.


KALLELSE TILL ÅRSSTÄMMA I XINTELA AB (PUBL)

Aktieägarna i Xintela AB (publ), org. nr. 556780-3480, kallas härmed till årsstämma den 7 maj 2021 kl. 09.00 i Medicon Village, Scheeletorget 1, hus 601, i Lund.


Xintela rapporterar positiva resultat från preklinisk ARDS studie och erhåller nytt anslag om 2,3 miljoner kronor

Lund, Sverige, 6 april, 2021 - Xintela meddelar idag positiva resultat från den prekliniska ARDS (Acute Respiratory Distress Syndrome) studien som delfinansierats av Vinnova. Resultaten från studien visar potentialen av bolagets stamcellsprodukt XSTEM® för behandling av ARDS, en livshotande lungkomplikation som bl.a. kan drabba svårt sjuka covid-19 patienter. Xintela meddelar också att bolaget har erhållit ett nytt bidrag från Swelife/Vinnova för att fortsätta undersöka verkningsmekanismer av XSTEM i ARDS modellen och förbereda XSTEM för kliniska studier.


Xintela reports positive results from preclinical ARDS study and new grant of 2.3 million SEK

Lund, Sweden, 6 April 2021 - Xintela today announces the positive outcome of the preclinical ARDS (Acute Respiratory Distress Syndrome) study partly financed by Vinnova. The results of the study demonstrate the potential of the company's stem cell product XSTEM® in the treatment of ARDS, a life-threatening lung complication that can affect severely ill COVID-19 patients. Xintela also announces a new grant from Swelife/Vinnova to further investigate the mechanism of action of XSTEM in the preclinical ARDS model and to prepare XSTEM for clinical studies.


Xintela erhåller tillstånd för vävnadsinrättning

Lund, Sverige, 19 mars 2021 - Xintela meddelar idag att bolaget har erhållit tillstånd för vävnadsinrättning från Läkemedelsverket för hantering av humana vävnader och celler avsedda för framställning av läkemedel.


Xintela gets tissue establishment license

Lund, Sweden, 19 March 2021 - Xintela announces today that the company has received a tissue establishment license from the Swedish Medical Products Agency for handling human tissues and cells for manufacturing medicinal products.


Xintela erhåller godkänt patent i Europa för sin stamcellsprodukt XSTEM

Lund, Sverige, 17 mars 2021 - Xintela meddelar att Europapatentverket (EPO) idag har godkänt patentansökan avseende bolagets stamcellsprodukt XSTEM® bestående av integrin α10β1-selekterade mesenkymala stamceller.


Xintela gets patent grant in Europe for XSTEM stem cell product

Lund, Sweden, 17 March 2021 - Xintela announces that the European Patent Office (EPO) has today approved the patent application for the company's stem cell product XSTEM® consisting of integrin 10-selected mesenchymal stem cells.


Xintela publicerar antikroppsresultat från glioblastomstudie

Lund, Sverige, 12 mars 2021 - Xintela meddelar att resultaten från bolagets prekliniska glioblastomstudie med funktionsblockerande antikroppar idag har publicerats i den välrenomerade internationella vetenskapliga tidskriften Cancers. Publikationen visar bland annat att antikroppar riktade mot bolagets målmolekyl integrin 101 signifikant minskar tillväxt av den mycket aggressiva hjärntumören glioblastom i en djurmodell.


Xintela publishes results from glioblastoma antibody study

Lund, Sweden, March 12, 2021 - Xintela announces that the results of the company's preclinical glioblastoma study with function-blocking antibodies have today been published in the renowned international scientific journal Cancers. The publication shows, among other things, that antibodies directed to the company's target molecule integrin 101 significantly reduce the growth of the aggressive and deadly brain tumor glioblastoma in an animal model.


Bokslutskommuniké 2020-01-01 till 2020-12-31

Sammanfattning av bokslutskommuniké


Year-end report 1 Jan - 31 Dec 2020

Summary of the year-end report


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