Table of contents
- Trial overview
- Condition and target population
- Study design and phase
- What is being measured
- Who may join the study
- Why this trial matters
Trial overview
This article covers one interventional study of SAR445399 in adults with moderate to severe hidradenitis suppurativa.[1] The study is listed as authorised and is a Phase 2 trial with a planned enrollment of 206 participants.[1]
Condition and target population
The trial is studying hidradenitis suppurativa (HS), a long-term skin condition, in adults who have moderate to severe disease.[1] This means the study is focused on people whose symptoms are not mild and who may need more active treatment research options.[1]
Study design and phase
The available data describe SAR445399 as part of a Phase 2 study.[1] Phase 2 trials are used to learn more about whether a treatment may work and to keep checking safety in a defined patient group.[1]
The study summary says it is evaluating different doses of SAR445399.[1] In simple terms, the researchers are comparing amounts of the study treatment to see how well they may help people with this condition.[1]
What is being measured
The main goal of the study is to evaluate efficacy, which means how well the treatment works for the target condition.[1] The trial also aims to assess safety, meaning whether the treatment can be used without causing unacceptable harm in the study setting.[1]
Because the brief summary specifically mentions efficacy of different doses, the study is likely focused on whether one dose works better than another for people with hidradenitis suppurativa.[1]
Who may join the study
The trial data state that the study is for adult participants with moderate to severe hidradenitis suppurativa.[1] No other eligibility details are provided in the source data, so the full set of entry rules cannot be confirmed here.[1]
Why this trial matters
Hidradenitis suppurativa can be difficult to manage when it is moderate to severe, so studies like this one are important for finding better treatment options.[1] This trial may help show whether SAR445399 is worth studying further in this patient group.[1]


