Hexaminolevulinate hydrochloride is under clinical development by Asieris Pharmaceuticals and currently in the Phase III 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 Hexaminolevulinate hydrochloride’s likelihood of approval (LoA) and phase transition for Cervical Intraepithelial Neoplasia (CIN) took place on 17 Aug 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 Hexaminolevulinate hydrochloride Likelihood of Approval (LoA) and Phase Transition Success Rate (PTSR) Report.

Hexaminolevulinate hydrochloride overview

Cevira (APL-1702) is under development for the treatment of cervical high grade squamous intraepithelial lesion (HSIL) caused by infection with all HPV subtypes. It is hexaminolevulinate (HAL) photodynamic therapy (PDT).

Asieris Pharmaceuticals overview

Asieris Pharmaceuticals discovers and develops drugs for the treatment of genitourinary tumors. The company is investigating APL-1202, an oral drug to treat non-muscle-invasive bladder cancer (NMIBC); APL-1702(Cevira), a photodynamic therapy against cervical high grade squamous intraepithelial lesion (HSIL); and APL-1706 (Hexvix), a fluorescent imaging agent to assist in the diagnosis of bladder cancer. It is also evaluating drugs for triple negative breast cancer, metastatic castration resistant prostate cancer, ER positive breast cancer and other reproductive diseases; autoimmune diseases; and Acinetobacter baumannii infection. Asieris Pharmaceuticals conducts research and development in the therapeutic areas of bladder cancer, oncology, multidrug-resistance infections and tumor immunotherapy. The company operates with additional offices in the US and China. Asieris Pharmaceuticals is headquartered in Pudong, China.

Quick View Hexaminolevulinate hydrochloride LOA Data

Report Segments
  • Innovator
Drug Name
  • Hexaminolevulinate hydrochloride
Administration Pathway
Therapeutic Areas
  • Women’s Health
Key Developers
Highest Development Stage
  • Phase III

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.