Organization (Industry)
CSL Behring GmbH
ClinicalTrials.gov lists CSL Behring GmbH as lead sponsor of 145 trials. It has 73 active development programs and 21 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: 5 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 7 in 2026 and about 8 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 CSL Behring GmbH: 145 lead-sponsored trials and 6 legal-entity registrations. Part of CSL LTD.
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 (116)
Shown in this order: most trials first.
| Disease area | Trials |
|---|---|
| Primary Immunodeficiency Diseases | 26 |
| Hemophilia B | 24 |
| Hemophilia A | 21 |
| Angioedema | 16 |
| Angioedemas, Hereditary | 16 |
Showing 5 of 116 disease areas.
Trials by start year as sponsor or collaborator (26)
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) | 5 |
| 2025 | 10 |
| 2024 | 10 |
| 2023 | 7 |
| 2022 | 5 |
| 2021 | 7 |
| 2020 | 11 |
| 2019 | 13 |
| 2018 | 11 |
| 2017 | 5 |
Showing 10 of 26 years.
Prediction, not a registry value: median of 36 months from start to primary completion across 13 trials still running at the 2026-10-09 snapshot; registered median of 23 months across 117 trials with a primary completion typed Actual. Source: ClinicalTrials.gov / AACT (CTTI), public domain.
Active development programs (73)
Shown in this order: max phase, then active trials.
| Drug | Disease area | Max phase | Trials |
|---|---|---|---|
| Cryoprecipitate | Afibrinogenemia | Phase 3 | 2 |
| Factor IX | Hemophilia B | Phase 3 | 2 |
| IgPro20 | Lymphoma | Phase 3 | 1 |
| IgPro20 | Multiple Myeloma | Phase 3 | 1 |
| IgPro20 | Lymphoma, Non-Hodgkin | Phase 3 | 1 |
Showing 5 of 73 active programs.
Approved assets (21)
Shown in this order: max phase first.
| Drug | Trials |
|---|---|
| CSL312 | 9 |
| IgPro20 | 8 |
| IgPro10 | 5 |
| Voncento | 2 |
| Vivaglobin | 2 |
Showing 5 of 21 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 |
|---|---|
| 58% hit target (n=48) | 38% on time (n=48) |
Journals published in (162)
Shown in this order: most published in first.
| Journal | Publications |
|---|---|
| Journal of clinical immunology | 13 |
| The New England journal of medicine | 13 |
| Journal of thrombosis and haemostasis : JTH | 11 |
| Blood | 10 |
| Transfusion | 10 |
Showing 5 of 162 journals.
US granted patents (1)
Patents are not classified by disease area in the source, so this is the organization's overall portfolio, not a split by disease.
| US patents granted | Granted in the last 5 years | Most recent grant |
|---|---|---|
| 100 | 15 | 2025-08-26 |
Organization relationships (87)
Shown in this order: most evidence first.
| Related organization | Relationship | Evidence |
|---|---|---|
| Parexel | Co sponsors trial with | 5 |
| Parexel | Uses vendor | 5 |
| Government of the United States of America | Co sponsors trial with | 4 |
| American Thrombosis and Hemostasis Network | Co sponsors trial with | 3 |
| Johann Wolfgang Goethe University Hospital | Co sponsors trial with | 3 |
Showing 5 of 87 relationships.
Latest dated events (1,024)
Shown in this order: newest first.
| Date | Event | Source |
|---|---|---|
| 2026-09-15 | Trial started | Clinical trials (ClinicalTrials.gov) (ClinicalTrials.gov, U.S. National Library of Medicine; AACT database, Clinical Trials Transformation Initiative (CTTI)) |
| 2026-07-31 | FDA inspection | FDA enforcement (warning and untitled letters, recalls, inspections, import refusals, debarment) |
| 2026-07-20 | Trial started | Clinical trials (ClinicalTrials.gov) (ClinicalTrials.gov, U.S. National Library of Medicine; AACT database, Clinical Trials Transformation Initiative (CTTI)) |
| 2026-07-17 | FDA inspection | FDA enforcement (warning and untitled letters, recalls, inspections, import refusals, debarment) |
| 2026-06-26 | FDA inspection | FDA enforcement (warning and untitled letters, recalls, inspections, import refusals, debarment) |
Showing 5 of 1,024 events.
Biomarker capability evidence (490)
Shown in this order: tier desc, then gene symbol.
| Gene | Role | Evidence |
|---|---|---|
| ABCC6 | Trial sponsor | Named in trial inclusion criteria |
| ABO | Trial sponsor | Named in trial inclusion criteria |
| ABR | Trial sponsor | Primary endpoint in a Phase 3 trial |
| ACTN1 | Trial collaborator | Named in trial inclusion criteria |
| APOH | Trial collaborator | Named in trial inclusion criteria |
Showing 5 of 490 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 inspection record, fda recalls, fda import refusals, manufacturing and distribution sites, climate targets, as filed, workforce and board diversity, as filed, clia clinical laboratory certificates, and biomarkers this organization publishes on.