US FDA grants QIDP designation to Affinium Pharma's staphylococcal-specific antibiotic, AFN-1252
The US Food and Drug Administration (FDA) has designated Affinium Pharmaceuticals' phase II antibiotic, AFN-1252, as a Qualified Infectious Disease Product (QIDP) for use in acute bacterial skin and skin structure infections (ABSSSI) based on the phase II study recently completed in that indication. The QIDP designation is expected to enable Affinium to benefit from FDA regulatory incentives for new antibiotics, including priority review, and a five year extension of new chemical entity exclusivity.
"We are very pleased to receive the QIDP designation for our ground-breaking staphylococcal-specific antibiotic, AFN-1252," says Dr Ed Mascioli, chief executive officer of Affinium. "It provides important acknowledgment that Staphylococcus continues to be a major pathogen with significant unmet needs."
In addition, Affinium also completed dosing of the planned IV phase I single ascending dose study of AFN-1720, the prodrug of AFN-1252. All planned cohorts for the phase I study were dosed and results will be available in the coming weeks.
AFN-1720 is a new prodrug of Affinium's successful clinical-stage drug, AFN-1252, and represents a new clinical-stage agent in this novel class of antibiotics. Due to the unique, staphylococcal-specific spectrum of AFN-1252, AFN-1720 is expected to preserve the human gut microbiome resulting in minimal antibiotic-associated side effects, such as antibiotic-induced diarrhoea or C. difficile overgrowth. Clinical data observed to date support this concept. Additionally, with no resistance pressure on other bacterial species, the development of multiple drug-resistant organisms like vancomycin-resistant enterococci (VRE) is unlikely. Oral and IV AFN-1720 are being developed for clinical use in several serious infections. AFN-1252, the parent molecule of AFN-1720, is 3-20 times more potent than linezolid in animal models of infection, and is exquisitely potent against all strains of Staphylococcus aureus, with an MIC90 of 0.016 µg/ml against 5,400 strains of Staphylococcus aureus tested to date including all known resistant strains such as MRSA and vancomycin-intermediate S. aureus (VISA). In clinical trials, AFN-1252 has demonstrated an excellent efficacy, safety and tolerability profile in over 250 subjects.
Staphylococcus is the mostly commonly identified bacterial pathogen in man and is a potential pathogen in almost every type of bacterial infection. Methicillin-resistant strains of S. aureus (MRSA) account for about half of all S. aureus strains in the US and cause significant morbidity and mortality worldwide. According to the Infectious Disease Society of America (IDSA), MRSA kills more Americans every year than emphysema, HIV/AIDS, Parkinson's disease and homicides combined.
Affinium Pharmaceuticals is a clinical-stage biopharmaceutical company focused on the development of novel anti-infective medicines based on bacterial fatty acid synthesis inhibition.