Panaecin is under clinical development by Aridis Pharmaceuticals and currently in Phase II for Cystic Fibrosis. According to GlobalData, Phase II drugs for Cystic Fibrosis have a 31% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Panaecin’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
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GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.
Panaecin overview
Panaecin (gallium citrate) is under development for the treatment of bacterial lung infections including Pseudomonas aeruginosa infections in patients with cystic fibrosis (CF), ventilator-associated pneumonia, S. aureus, methicillin-resistant S. aureus (MRSA), B. cepacia, cystic fibrosis and COPD exacerbation. It is administered to the lung by inhalation route and through topical route in wound infections. Panaecin is developed based on inhalable aerosols technology. It was also under development for the treatment of wounds infection
Aridis Pharmaceuticals overview
Aridis Pharmaceuticals (Aridis) is a biopharmaceutical company. The company’s pipeline products include AR-301 (tosatoxumab ), AR-320 (suvratoxumab), AR-501 (Gallium Citrate), AR-701 (COVID-19 mAb). AR-301 (tosatoxumab) is a Human anti-S. aureus mAb for therapeutic treatment of VAP, AR-320 (suvratoxumab) is a Long-acting human anti-S. aureus for prevention of VAP, AR-501 (Gallium Citrate) is a novel anti-infective for the growing problem of antibiotic resistance, AR-701 (COVID-19 mAb) Human mAb Cocktail to SARS-CoV-2 Virus. The company also works on macromolecular stabilization technology to increase the stability of vaccines. Aridis is headquartered in San Jose, California, the US.
For a complete picture of Panaecin’s drug-specific PTSR and LoA scores, buy the report here.
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GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article.
GlobalData’s Likelihood of Approval analytics tool dynamically assesses and predicts how likely a drug will move to the next stage in clinical development (PTSR), as well as how likely the drug will be approved (LoA). This is based on a combination of machine learning and a proprietary algorithm to process data points from various databases found on GlobalData’s Pharmaceutical Intelligence Center.
