DGAP-News: AiCuris received approval from BfArM to initiate Compassionate Use Program for Pritelivir in Germany

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DGAP-News: AiCuris Anti-infective Cures GmbH / Key word(s): Study
AiCuris received approval from BfArM to initiate Compassionate Use Program for Pritelivir in Germany

02.12.2020 / 10:00
The issuer is solely responsible for the content of this announcement.


AiCuris receives approval from BfArM to initiate Compassionate Use Program for Pritelivir in Germany

  • The Compassionate Use Program (CUP) may provide access to pritelivir for use in immunocompromised patients that have acyclovir-resistant mucocutaneous herpes simplex virus infections and foscarnet resistance or intolerance
  • CUPs offer a method to provide patients suffering from an unmet medical need and with no further treatment options with possible access to medication currently not approved in their home country
  • The today announced approval is part of an Early Access Program (EAP) for Pritelivir in various countries throughout the world

WUPPERTAL, Germany, December 02, 2020 - AiCuris Anti-infective Cures GmbH, a leading company in the discovery and development of drugs against infectious diseases, today announced the approval from the German "Bundesinstitut für Arzneimittel und Medizinprodukte (BfArM)" to initiate a Compassionate Use Program (Härtefallprogramm) for pritelivir for the treatment of immunocompromised patients who have acyclovir-resistant mucocutaneous herpes simplex virus (HSV) infections and in addition foscarnet resistance or intolerance. AiCuris is currently preparing a pivotal Phase 3 trial with pritelivir in immunocompromised patients whose HSV infections have become resistant to acyclovir as a basis for NDA submission.

"Especially in immunocompromised patients, HSV can lead to serious complications," said Dr. Holger Zimmermann, CEO of AiCuris. "We are very happy that with this program we can give seriously ill patients with no further treatment options access to Pritelivir, a novel and resistance breaking therapeutic agent, and thus again hope. At the same time, the data collected in this program will help to bring the drug to patients as quickly as possible and support the planned approval of pritelivir."

Compassionate use is a treatment option that allows the use of an unauthorised medicine for the treatment of patients who have a disease which cannot be treated satisfactorily with any currently authorised medicine and who cannot enter clinical trials. These programs are only put in place if there is sufficient evidence of the effectiveness and safety of the drug and if the medicine is expected to help patients with life-threatening, long-lasting or seriously debilitating illnesses.

The Compassionate Use Program in Germany is part of an Early Access Program (EAP) which is operated by myTomorrows, a Netherlands-based HealthTech company facilitating access to medicines in development and real-world data collection. The EAP for treatment of acyclovir-resistant mucocutaneous HSV infections provides immunocompromised patients in different countries worldwide with pre-approval access to pritelivir.


About Pritelivir

Pritelivir is an innovative, highly active and specific inhibitor of herpes simplex virus (HSV). Derived from a novel chemical class (thiazolylamides), pritelivir is active against both types of herpes simplex virus (HSV-1 and HSV-2), causing labial and genital herpes, and retains activity against viruses which have become resistant to marketed drugs. Pritelivir has a novel mode of action that is distinct from other antiviral agents currently in use for treating HSV infections (i.e., the nucleoside analogs acyclovir and its prodrug valacyclovir as well as famciclovir, the prodrug of penciclovir). While nucleoside analogs terminate ongoing DNA chain elongation through inhibition of viral DNA polymerase, pritelivir prevents de novo synthesis of viral DNA through inhibition of the helicase-primase complex. In addition, it does not require activation within an HSV infected cell by viral thymidine kinase and is therefore also protective to uninfected cells.

Pritelivir, showed superiority against standard treatment valacyclovir in a clinical Phase 2 trial in patients with genital HSV-2 infection and is currently in a Phase 2 clinical trial in the U.S., to assess efficacy and safety comparing pritelivir to i.v. foscarnet, a virostatic agent which is used mainly for the treatment of HSV resistant to other antiviral drugs. In June 2020, AiCuris was granted Breakthrough Therapy Designation by U.S. FDA for Pritelivir for the treatment of HSV infections in immunocompromised patients. Based on early results from the ongoing clinical Phase 2 study, AiCuris is in close communication with the FDA and preparing a pivotal Phase 3 trial as a basis for NDA submission.


About HSV

Herpes simplex viruses are widespread (seroprevalence up to 100%, depending on geographic area and subpopulation) and are divided into herpes simplex virus type 1 (HSV-1) and type 2 (HSV-2). Infections lead to lifelong persistence of the virus, with frequent and sometimes painful recurrences. While HSV-1 predominantly causes oral lesions (cold sores), HSV-2 manifests in the genital region and is mainly sexually transmitted. In immunocompromised patients, HSV can lead to serious complications. The negative stigma associated with genital herpes and visible facial lesions may cause psychological distress.

According to the World Health Organization (WHO), an estimated 491 million people aged 15-49 (13%) worldwide were living with genital herpes caused by HSV-2 in 2016. Prevalence of HSV-2 infection was estimated to be highest in Africa (44% in women and 25% in men), followed by the Americas (24% in women and 12% in men ). It was also shown to increase with age, although the highest numbers of newly infected people were adolescents.


About Compassionate Use Program (CPU)

A Compassionate Use Program, supports in a compliant and controlled way the treatment with a medicine currently not licensed in a patient's country of residence. Such treatment can be an option for patients who have high unmet medical needs, have exhausted all registered treatment options and cannot participate in a clinical trial.


About AiCuris Anti-infective Cures GmbH

AiCuris was founded in 2006 as a spin-off from Bayer and focuses on the discovery and development of drugs targeting infectious diseases. SANTO Holding is the Company's majority investor. PREVYMIS(R) (Letermovir), a first-in-class non-nucleoside cytomegalovirus (CMV) inhibitor acting via a novel mechanism of action, was licensed to MSD in 2012 and is approved in the EU, the USA, Japan and other parts of the world for use in bone marrow transplants for the prevention of HCMV infections in adults who receive an allogeneic hematopoietic stem cell transplant. The Company is developing drugs for the treatment of viruses such as human CMV, herpes simplex virus (HSV), hepatitis B virus (HBV), and adenoviruses. In the field of antibacterials, AiCuris seeks to develop innovative treatment options for life-threatening, multidrug-resistant, hospital-treated pathogens.

In 2018 Dr. Holger Zimmermann, CEO of AiCuris, and Prof. Dr. Helga Rübsamen-Schaeff, Founding CEO, were awarded the German Future Prize 2018 (German President's Award for Innovation in Science and Technology) for the development of Letermovir and their project, "Protection in the Absence of the Immune System - a Life-Saving Innovation against Dangerous Viruses" (original title: "Schutz bei fehlendem Immunsystem - die lebensrettende Innovation gegen gefährliche Viren").

For more information, please visit www.aicuris.com.
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For inquiries on Early Access to pritelivir, please contact myTomorrows via aicuris.medical@mytomorrows.com.


Contacts:

Company:

AiCuris Anti-infective Cures GmbH


Katja Woestenhemke
Phone: +49 202 317 63 0

Email: press@aicuris.com
Media relations:

MC Services AG


Dr. Solveigh Mähler
Phone: +49 211 529 252 19

E-Mail: aicuris@mc-services.eu


02.12.2020 Dissemination of a Corporate News, transmitted by DGAP - a service of EQS Group AG.
The issuer is solely responsible for the content of this announcement.

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