Lebrikizumab is under clinical development by Eli Lilly and Co and currently in Pre-Registration for Atopic Dermatitis (Atopic Eczema). According to GlobalData, Pre-Registration drugs for Atopic Dermatitis (Atopic Eczema) have an 87% phase transition success rate (PTSR) indication benchmark for progressing into Marketed. GlobalData’s report assesses how Lebrikizumab’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.

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.

Lebrikizumab overview

Lebrikizumab (RG-3637, RO-5490255, MILR-1444A, PRO-301444, TNX-650) is under development for the treatment of persistant moderate to severe atopic dermatitis and idiopathic pulmonary fibrosis. It is administered by subcutaneous route. The drug candidate is an interleukin (IL)-13 antibody. It was also under development for severe asthma and chronic obstructive pulmonary disease.

Eli Lilly and Co overview

Eli Lilly and Co (Lilly) is a healthcare company that is engaged in the discovery, development, and marketing of human healthcare products. The company offers medicines for cardiovascular conditions, diabetes, endocrinology, cancer, neurological problems, immune disorders, men’s health and musculoskeletal problems. The company distributes its pharmaceutical health products through independent wholesale distributors. Lilly conducts research and development activities to discover and deliver innovative medicines. It also promotes products through sales representatives and marketing agreements with other pharmaceutical companies. The company also offers its products in North America, South America, Europe, South Asia, the Middle East, Africa and North Asia-Pacific. Lilly is headquartered in Indianapolis, Indiana, the US.

For a complete picture of Lebrikizumab’s drug-specific PTSR and LoA scores, buy the report here.


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.