Organization (Industry)
Leo Pharma (France)
ClinicalTrials.gov lists Leo Pharma (France) as lead sponsor of 225 trials. It has 136 active development programs and 49 approved assets.
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Trials started per year with this organization as sponsor or collaborator, 1990 onward. The series also counts trials where the organization is a collaborator; the lead-sponsor trial count does not.
2026 is partial: 2 registered with a 2026 start date. The hollow diamonds on the dashed line are a forecast of the full-year count, planned starts included: about 3 in 2026 and about 5 in 2027, the average of the 24 months through September, counted as registered and carried forward. The columns, the lighter one included, count trials registered so far with a start date in the year, planned starts included; the forecast looks ahead to the count for the whole year, so it is not the same measure. This method has not been backtested on organizations. In backtests on conditions with as many trial starts a year as this organization (5 to 20), forecasts made part-way through the year were typically off by about 28 percent and ran about 20 percent low against the count later registered; forecasts made before the year began were off by about 39 percent and ran about 37 percent low against the count later registered. These figures rest on a few years of history (target years from 2018 to 2025, varying by figure), place each condition as it is mapped today rather than as it was then, and score against a count for the newest year that was still being revised. Only condition series were scored.
This page covers Leo Pharma (France): 225 lead-sponsored trials and 6 legal-entity registrations. The parent company on record for Leo Pharma (France) is LEO Foundation, which does not have its own page on this site.
Related companies are recorded in the same corporate group by GLEIF, ROR or a curator but are not grouped here; they are listed below with their own counts and are not included in the figures above.
Disease areas (72)
Shown in this order: most trials first (counted at this company's own legal-entity record, not the consolidated group).
| Disease area | Trials |
|---|---|
| Dermatitis, Atopic | 44 |
| Keratosis, Actinic | 40 |
| Psoriasis | 20 |
| Thrombosis | 14 |
| Thromboembolism | 11 |
Showing 5 of 72 disease areas.
Trials by start year as sponsor or collaborator (29)
Shown in this order: most recent first. 2026 is partial: trials registered with a 2026 start date so far, not a full year.
Show the table of trials by start year as sponsor or collaborator
| Year | Trials started |
|---|---|
| 2026 (partial year) | 2 |
| 2025 | 7 |
| 2024 | 1 |
| 2023 | 9 |
| 2022 | 12 |
| 2021 | 13 |
| 2020 | 5 |
| 2019 | 13 |
| 2018 | 19 |
| 2017 | 15 |
Showing 10 of 29 years.
Prediction, not a registry value: median of 30 months from start to primary completion across 5 trials still running at the 2026-10-09 snapshot; registered median of 9 months across 204 trials with a primary completion typed Actual. Source: ClinicalTrials.gov / AACT (CTTI), public domain.
Active development programs (136)
Shown in this order: max phase, then active trials.
| Drug | Disease area | Max phase | Trials |
|---|---|---|---|
| Delgocitinib | Lichen Sclerosus et Atrophicus | Phase 3 | 1 |
| Cream Vehicle | Lichen Sclerosus et Atrophicus | Phase 3 | 1 |
| Spesolimab | Pyoderma Gangrenosum | Phase 3 | 1 |
| Tralokinumab + TCS | Dermatitis, Atopic | Phase 3 | 1 |
| PREDNISOLONE | Pyoderma Gangrenosum | Phase 3 | 1 |
Showing 5 of 136 active programs.
Approved assets (49)
Shown in this order: max phase first.
| Drug | Trials |
|---|---|
| Azelaic Acid | 5 |
| Ingenol Mebutate Gel, 0.015% | 4 |
| Brodalumab | 4 |
| Azelaic Acid 15% Gel | 3 |
| Xamiol® Gel | 3 |
Showing 5 of 49 approved assets.
Sponsor delivery record (1)
Enrollment hit target: the share of this sponsor's lead-sponsored trials whose actual enrollment reached the planned enrollment. On time: the share whose actual primary completion date was no later than the planned date. Each share counts only trials where we observed an estimated figure before the actual one, and n is that number of trials. Below 5 trials the count is shown as a fraction, not a percentage.
| Enrollment | Timeline |
|---|---|
| 61% hit target (n=57) | 48% on time (n=58) |
FDA inspection record (1)
| Latest classification | Inspections |
|---|---|
| VAI | 6 |
FDA import refusals (1)
| Refused import lines | Latest refusal |
|---|---|
| 17 | 2024-10-08 |
Manufacturing and distribution sites (2)
Shown in this order: severity rank then name.
| Facility | Location | Regulators | Member organization |
|---|---|---|---|
| LEO Pharma A/S | Ballerup, DK | EMA, FDA, Health Canada | |
| Leo Pharma A/S | Esbjerg Oe, DK | EMA, Health Canada |
Biomarker capability evidence (257)
Shown in this order: tier desc, then gene symbol.
| Gene | Role | Evidence |
|---|---|---|
| ALB | Trial sponsor | Named in trial inclusion criteria |
| ALB | Trial sponsor | Named in trial inclusion criteria |
| ALB | Trial sponsor | Named in trial inclusion criteria |
| ALB | Trial sponsor | Named in trial inclusion criteria |
| ALB | Trial sponsor | Named in trial inclusion criteria |
Showing 5 of 257 evidence rows.
Not on this page
Checked, with nothing recorded for this organization: companies grouped under this page, sec-reported annual financials, financing and grant events, fda warning letters, fda untitled letters, fda recalls, climate targets, as filed, workforce and board diversity, as filed, organization relationships, and clia clinical laboratory certificates.
Counted at group level under LEO Foundation: journals published in, us granted patents, latest dated events, and biomarkers this organization publishes on.