THERAVECTYS presenteert resultaten van onderzoek naar eerste vaccintherapie op basis van lentivirale vectoren op HIV Cure Symposium
PARIS–(BUSINESS WIRE)–THERAVECTYS, een in Parijs gevestigd volledig geïntegreerd bedrijf in onderzoek naar en klinische ontwikkeling van lentivirale therapeutische vaccins en t-celtherapieën, heeft vandaag bekendgemaakt dat het gedetailleerde resultaten van zijn eerste- en tweedefaseonderzoek presenteert op het symposium Towards an HIV Cure, dat op 18 en 19 juli plaatsvindt in Vancouver en voorafgaat aan de achtste IAS Conference on HIV Pathogenesis, Treatment & Prevention (IAS 2015). Aan het gerandomiseerde, placebogecontroleerde onderzoek (ClinicalTrials.gov Identifier: NCT02054286) werken op het moment 38 hiv-positieve patiënten mee. De proef vergelijkt drie verschillende doses van een therapeutisch kandidaatsvaccin met een placebo op gebied van veiligheid, verdraagbaarheid en immunogeniciteit. De behandeling bestaat uit twee intramusculaire injecties met een tussenpoos van acht weken van niet-repliceerbare en zelfactiverende lentivirale vectoren die immunogenetische regionen van de proteïnen HIV GAG, POL en NEF activeren.
THERAVECTYS to Present Detailed Phase I/II Results from the First-Ever Lentiviral-Vector Based Therapeutic Vaccine Trial at the 2015 Towards an HIV Cure Symposium
PARIS–(BUSINESS WIRE)–THERAVECTYS, a Paris-based, fully-integrated discovery & clinical development company specialized in lentiviral vector-based therapeutic vaccines and T-cell therapies announced that detailed results from its phase I/II study will be presented at the 2015 Towards an HIV Cure Symposium in Vancouver, Canada, on 18 & 19 July 2015, immediately preceding the 8 th IAS Conference on HIV Pathogenesis, Treatment & Prevention (IAS 2015). The randomized, placebo-controlled trial (ClinicalTrials.gov Identifier: NCT02054286) currently enrolled 38 HIV-positive patients under HAART and aimed at comparing the safety, tolerability and immunogenicity of the therapeutic vaccine candidate at 3 different doses (5.106, 5.107 or 5.108 TU) versus placebo. The treatment regimen consisted of two intramuscular injections 8 weeks apart with non-replicative and self-inactivating lentiviral vectors encoding for immunogenic regions of the HIV GAG, POL and NEF proteins. Vaccine-induced HIV-1-antigen-specific T-cell in peripheral blood were characterized by intracellular cytokine staining in all patients, placebo included, before and after HAART interruption 24 weeks after the first injection
“We are very pleased to present the clinical data of this first-ever lentivector based therapeutic vaccine trial” says Dr. Hélène TOUSSAINT, senior scientist in charge of the HIV vaccine program. With the absence of any serious adverse events on all 38 patients and no safety concerns related to the treatment, the clinical data confirmed both safety and tolerance of the lentiviral-based therapeutic vaccine. In addition, the analysis of the immunological data demonstrated the ability of the vaccine candidate to elicit multi-specific and poly-functional CD8 and CD4 T-cell responses in most of the vaccinated patients.
“These data provide further evidence that THERAVECTYS’ regimen vaccine is safe and well tolerated, and can induce intense, broad and long-lasting cellular immune responses in vaccinated patients regardless their preexisting immune profile” says Dr. Cécile BAUCHE, Chief Scientific Officer of the Company. In this trial, a high frequency, from 0.097 to 0.874%, of functional T-cells able to produce at least 2 or 3 cytokines among IFN-γ, TNF-α and IL-2 was evidenced across patients. A dose effect was also observed when comparing the 3 groups, with greater magnitude with the highest dose.
“The clinical data of this trial supports the potential of the lentiviral vector platform developed by THERAVECTYS for the future development of therapeutic vaccines and immunotherapies in oncology and infectious diseases.” says Renaud VAILLANT, Chief Executive Officer, THERAVECTYS.
For a complete review of THERAVECTYS’ technologies & programs, please visit the company’s website.
About THERAVECTYS
THERAVECTYS is a
fully-integrated discovery and clinical development biotech company originating from the Pasteur Institute. Based on its lentiviral vector technology platform, THERAVECTYS develops therapeutic vaccines and immunotherapies to fight cancers and infectious diseases, including a proprietary and differentiated CAR T-cell technology platform.
Capitalizing over 15 years of fundamental research in the field of lentiviral vectors, the company has built a broad and robust intellectual property position in addition to worldwide and exclusive licenses secured from institutions including Institut Pasteur and Institut Curie.
The company’s lead infectious disease lentivector vaccine has successfully completed a Phase I/II safety & immunogenicity human proof-of-concept study in HIV. THERAVECTYS lead oncology lentivector vaccine will enter clinical trials in 2015 while the company’s CAR T-cell therapies are in the preclinical stage.
Alone or with partners, THERAVECTYS plans to advance its pipeline of oncology and infectious disease therapies using the company’s integrated set of discovery, clinical development, and GMP manufacturing capabilities specialized in lentiviral vector technologies.
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Contacts
THERAVECTYS
Audrey Bonafos, +33 1 43 90 19 20
press@theravectys.com