AVTX-002 is under clinical development by Avalo Therapeutics and currently in the Phase II in clinical pathway. The characteristics of the clinical trial as well as other attributes related to the drug, regulations, and company play a fundamental role in ensuring the likelihood of transition that the drug moves from its current development stage to next.

According to GlobalData, the latest event to affect AVTX-002’s likelihood of approval (LoA) and phase transition for Asthma took place on 13 Sep 2022, which increased the likelihood that the drug progresses to the next phase in its clinical pathway and increased the likelihood of final approval for this indication.

GlobalData uses proprietary data and analytics to provide a complete picture of this assessment in their AVTX-002 Likelihood of Approval (LoA) and Phase Transition Success Rate (PTSR) Report.

AVTX-002 overview

AVTX-002 (AEVI-002, KHK-252067,SAR-252067) is under development for the treatment of severe pediatric onset Crohn’s disease, moderate to severe Crohn's disease, COVID-19 cytokine storm induced acute respiratory distress syndrome, pneumonia, acute lung injury and non-eosinophilic asthma (NEA). It is administered through subcutaneous route. It is a fully human anti-light monoclonal antibody. LIGHT is a tumor necrosis factor (TNF) super-family member that is implicated as a key mediator of inflammation.

It was under development for the treatment of ulcerative colitis.

Avalo Therapeutics overview

Avalo Therapeutics, formerly Cerecor is a biopharmaceutical company that develops and commercializes novel products in the fields of neurology and pediatrics. The company’s products include prescription medications, prescription devices and dietary supplements. Its pipeline products offer treatment in the areas of neurogenic orthostatic hypotension, parkinsons disease, seizures in epilepsy and deoxyguanosine kinase deficiency. Avalo Therapeutics‘ prescription medications comprise aciphex sprinkle, cefaclor, millipred tablets and dose packs and millipred oral solution, among others. The company also offers dietary supplements such as chewable tablets and drops. Avalo Therapeutics is headquartered in Baltimore, Maryland, the US.

Quick View AVTX-002 LOA Data

Report Segments
  • Innovator
Drug Name
  • AVTX-002
Administration Pathway
  • Subcutaneous
Therapeutic Areas
  • Gastrointestinal
  • Infectious Disease
  • Respiratory
Key Developers
  • Sponsor Company: Avalo Therapeutics
  • Originator: La Jolla Institute for Immunology and Kyowa Kirin
Highest Development Stage
  • Phase II

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 its clinical pathway (PTSR), as well as how likely the drug will be approved (LoA). This is based on a proprietary algorithm built from the drugs’ sales forecast, regulatory milestones, cost forecasts, WACC rate and other proprietary data sources found on GlobalData’s Pharmaceutical Intelligence Center.