BAGNEUX, France I December 7, 2015 I DBV Technologies (Euronext: DBV – ISIN: FR0010417345 – Nasdaq Stock Market: DBVT), a clinical-stage specialty biopharmaceutical company, today announced the initiation of a pivotal Phase III study designed to evaluate the safety and efficacy of Viaskin(R) Peanut 250 micrograms in children ages 4 to 11 with peanut allergy. The Viaskin Peanut patch is the company’s lead product candidate, which is based on epicutaneous immunotherapy (EPIT(R)), a proprietary technology platform that can safely deliver biologically active compounds to the immune system through the immune cells of the intact skin.
PEPITES (Peanut EPIT(R) Efficacy and Safety Study), is an international, randomized 2:1, double-blind, placebo-controlled Phase III study, in which pediatric peanut allergic patients will be treated with Viaskin Peanut 250 micrograms or placebo for 12 months. During the trial, patients’ peanut allergy will be assessed using a double-blind, placebo controlled food challenge (DBPCFC) at baseline. Both the US Food and Drug Administration (FDA) and the European Medicines Agency (EMA) have agreed to a combined primary endpoint based on a responder analysis after 12 months of treatment. For patients with a baseline peanut protein eliciting dose (ED) equal to or less than 10 mg, a responder will be defined as a patient with a peanut protein ED equal to or greater than 300 mg of peanut protein after 12 months of treatment. For subjects with a baseline ED greater than 10 mg, a responder will be defined as a patient with a peanut protein eliciting dose equal to or greater than 1,000 mg of peanut protein after 12 months of treatment.
PEPITES is expected to enroll approximately 330 patients in about 30 centers across North America (Canada and the United States), Europe, and Australia. Following conversations with clinical centers and regulatory agencies, the company has decided to increase the size of its Phase III study in order to meet patient and investigator demand for Viaskin Peanut, as well as further strengthening the study’s ability to detect a clinically meaningful and statistically significant effect of Viaskin Peanut 250 micrograms. PEPITES is designed to confirm Viaskin Peanut’s treatment efficacy as shown in VIPES and OLFUS-VIPES, the company’s Phase IIb and open label follow-up studies. DBV also intends, following additional consultation with regulatory agencies, to conduct additional clinical trials, notably in both pediatric and adult patients that will define the efficacy and safety profile of Viaskin Peanut in a broad patient population.
Dr. Pierre-Henri Benhamou, Chairman & Chief Executive Officer of DBV Technologies, said: “Over the last two decades, peanut allergic patients have been waiting for a treatment that could safely protect them against life-threatening anaphylaxis without causing dangerous side effects. If PEPITES’ results are in-line with data from our previous studies, we believe that Viaskin Peanut may be poised to be the first new therapy for safely treating peanut allergy.” Dr. Benhamou continued, “We are thankful for our patients, investigators and investors’ support throughout this development journey. In light of the demand for the patch at our clinical centers, we anticipate that we will complete PEPITES’ recruitment as originally planned, by the end of the third quarter of 2016.”
About PEPITES
During the Peanut EPIT(R) Efficacy and Safety Study (PEPITES), patients will be assessed using a double-blind, and placebo controlled food challenge (DBPCFC). Patients will be randomized 2:1 to receive either Viaskin Peanut 250 micrograms or placebo for 12 months. The combined primary endpoint is based on a responder analysis after 12 months of treatment with Viaskin Peanut 250 micrograms. For patients with a baseline peanut protein eliciting dose (ED) equal to or less than 10 mg, a responder is defined as a patient with a peanut protein ED equal to or greater than 300 mg of peanut protein after 12 months of treatment. For subjects with a baseline ED greater than 10 mg, a responder will be defined as a patient with a peanut protein eliciting dose equal to or greater than 1,000 mg of peanut protein after 12 months of treatment. As a secondary efficacy endpoint, Cumulative Reactive Dose (CRD) will also be used in PEPITES to establish the total quantity of peanut protein that triggers patient reactions at month 12 versus placebo. Serological markers will also be measured at baseline, 3, 6, and 12 months in order to characterize the immunological changes in patients.
About DBV Technologies
DBV Technologies created the Viaskin(R) patch, a proprietary technology platform with broad potential applications in immunotherapy. Viaskin is based on epicutaneous immunotherapy, or EPIT(R), DBV’s method of delivering biologically active compounds to the immune system through intact skin while avoiding compound transfer to the blood. With this new class of self-administered and non-invasive product candidates, the company is dedicated to safely transforming the care of food allergy patients, for which there are currently no approved treatments. DBV’s food allergy programs include ongoing clinical studies with Viaskin Peanut and Viaskin Milk, one experimental program with Viaskin Egg and a human proof concept clinical study in Eosinophilic Esophagitis. DBV is also exploring platform indications in vaccines, and selected immune diseases with unmet medical needs.
DBV Technologies has global headquarters in Paris, France and New York, NY, USA. Company shares are traded on segment B of Euronext Paris (Ticker: DBV, ISIN code: FR0010417345), part of the SBF120 index, and traded on the Nasdaq Global Select Market in the form of American Depositary Shares (each representing one-half of one ordinary share) (DBVT). For more information on DBV Technologies, please visit our website: www.dbv-technologies.com.
SOURCE: DBV Technologies
Post Views: 64
BAGNEUX, France I December 7, 2015 I DBV Technologies (Euronext: DBV – ISIN: FR0010417345 – Nasdaq Stock Market: DBVT), a clinical-stage specialty biopharmaceutical company, today announced the initiation of a pivotal Phase III study designed to evaluate the safety and efficacy of Viaskin(R) Peanut 250 micrograms in children ages 4 to 11 with peanut allergy. The Viaskin Peanut patch is the company’s lead product candidate, which is based on epicutaneous immunotherapy (EPIT(R)), a proprietary technology platform that can safely deliver biologically active compounds to the immune system through the immune cells of the intact skin.
PEPITES (Peanut EPIT(R) Efficacy and Safety Study), is an international, randomized 2:1, double-blind, placebo-controlled Phase III study, in which pediatric peanut allergic patients will be treated with Viaskin Peanut 250 micrograms or placebo for 12 months. During the trial, patients’ peanut allergy will be assessed using a double-blind, placebo controlled food challenge (DBPCFC) at baseline. Both the US Food and Drug Administration (FDA) and the European Medicines Agency (EMA) have agreed to a combined primary endpoint based on a responder analysis after 12 months of treatment. For patients with a baseline peanut protein eliciting dose (ED) equal to or less than 10 mg, a responder will be defined as a patient with a peanut protein ED equal to or greater than 300 mg of peanut protein after 12 months of treatment. For subjects with a baseline ED greater than 10 mg, a responder will be defined as a patient with a peanut protein eliciting dose equal to or greater than 1,000 mg of peanut protein after 12 months of treatment.
PEPITES is expected to enroll approximately 330 patients in about 30 centers across North America (Canada and the United States), Europe, and Australia. Following conversations with clinical centers and regulatory agencies, the company has decided to increase the size of its Phase III study in order to meet patient and investigator demand for Viaskin Peanut, as well as further strengthening the study’s ability to detect a clinically meaningful and statistically significant effect of Viaskin Peanut 250 micrograms. PEPITES is designed to confirm Viaskin Peanut’s treatment efficacy as shown in VIPES and OLFUS-VIPES, the company’s Phase IIb and open label follow-up studies. DBV also intends, following additional consultation with regulatory agencies, to conduct additional clinical trials, notably in both pediatric and adult patients that will define the efficacy and safety profile of Viaskin Peanut in a broad patient population.
Dr. Pierre-Henri Benhamou, Chairman & Chief Executive Officer of DBV Technologies, said: “Over the last two decades, peanut allergic patients have been waiting for a treatment that could safely protect them against life-threatening anaphylaxis without causing dangerous side effects. If PEPITES’ results are in-line with data from our previous studies, we believe that Viaskin Peanut may be poised to be the first new therapy for safely treating peanut allergy.” Dr. Benhamou continued, “We are thankful for our patients, investigators and investors’ support throughout this development journey. In light of the demand for the patch at our clinical centers, we anticipate that we will complete PEPITES’ recruitment as originally planned, by the end of the third quarter of 2016.”
About PEPITES
During the Peanut EPIT(R) Efficacy and Safety Study (PEPITES), patients will be assessed using a double-blind, and placebo controlled food challenge (DBPCFC). Patients will be randomized 2:1 to receive either Viaskin Peanut 250 micrograms or placebo for 12 months. The combined primary endpoint is based on a responder analysis after 12 months of treatment with Viaskin Peanut 250 micrograms. For patients with a baseline peanut protein eliciting dose (ED) equal to or less than 10 mg, a responder is defined as a patient with a peanut protein ED equal to or greater than 300 mg of peanut protein after 12 months of treatment. For subjects with a baseline ED greater than 10 mg, a responder will be defined as a patient with a peanut protein eliciting dose equal to or greater than 1,000 mg of peanut protein after 12 months of treatment. As a secondary efficacy endpoint, Cumulative Reactive Dose (CRD) will also be used in PEPITES to establish the total quantity of peanut protein that triggers patient reactions at month 12 versus placebo. Serological markers will also be measured at baseline, 3, 6, and 12 months in order to characterize the immunological changes in patients.
About DBV Technologies
DBV Technologies created the Viaskin(R) patch, a proprietary technology platform with broad potential applications in immunotherapy. Viaskin is based on epicutaneous immunotherapy, or EPIT(R), DBV’s method of delivering biologically active compounds to the immune system through intact skin while avoiding compound transfer to the blood. With this new class of self-administered and non-invasive product candidates, the company is dedicated to safely transforming the care of food allergy patients, for which there are currently no approved treatments. DBV’s food allergy programs include ongoing clinical studies with Viaskin Peanut and Viaskin Milk, one experimental program with Viaskin Egg and a human proof concept clinical study in Eosinophilic Esophagitis. DBV is also exploring platform indications in vaccines, and selected immune diseases with unmet medical needs.
DBV Technologies has global headquarters in Paris, France and New York, NY, USA. Company shares are traded on segment B of Euronext Paris (Ticker: DBV, ISIN code: FR0010417345), part of the SBF120 index, and traded on the Nasdaq Global Select Market in the form of American Depositary Shares (each representing one-half of one ordinary share) (DBVT). For more information on DBV Technologies, please visit our website: www.dbv-technologies.com.
SOURCE: DBV Technologies
Post Views: 64
