Organization (Industry)
INSMED Inc
ClinicalTrials.gov lists INSMED Inc as lead sponsor of 52 trials, counting the companies grouped under it. INSMED Inc itself has 23 active development programs and 10 approved assets.
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Trials started per year with this organization as sponsor or collaborator, 1990 onward. Companies grouped under this one are not included. The series also counts trials where the organization is a collaborator; the lead-sponsor trial count does not.
2026 is partial: 7 registered with a 2026 start date. The dashed outline is the pace from the 5 registered with a start date through September, planned starts included, not adjusted; not a forecast. No forecast is made for this organization: it averages 4.4 trial starts a year over the five years to September, under the 5 a year the method needs.
This page covers INSMED Inc and 1 company grouped under it: 52 lead-sponsored trials (50 its own, 2 in the grouped companies) and 3 legal-entity registrations (3 its own, 0 in the grouped companies).
Companies grouped under this page (1)
| Company | Lead trials | Legal entities |
|---|---|---|
| Insmed Gene Therapy LLC | 2 | 0 |
Disease areas (23)
Shown in this order: most trials first.
| Disease area | Trials |
|---|---|
| Hypertension, Pulmonary | 9 |
| Cystic Fibrosis | 8 |
| Lung Diseases, Interstitial | 6 |
| Hypertension | 5 |
| Mycobacterium Infections, Nontuberculous | 5 |
Showing 5 of 23 disease areas.
Trials by start year as sponsor or collaborator (17)
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) | 7 |
| 2025 | 1 |
| 2024 | 2 |
| 2023 | 8 |
| 2022 | 5 |
| 2021 | 4 |
| 2020 | 4 |
| 2019 | 1 |
| 2017 | 1 |
| 2016 | 2 |
Showing 10 of 17 years.
Prediction, not a registry value: median of 36 months from start to primary completion across 5 trials still running at the 2026-10-09 snapshot; registered median of 12 months across 37 trials with a primary completion typed Actual. Source: ClinicalTrials.gov / AACT (CTTI), public domain.
Active development programs (23)
Shown in this order: max phase, then active trials.
| Drug | Disease area | Max phase | Trials |
|---|---|---|---|
| Treprostinil Palmitil Inhalation Powder | Hypertension, Pulmonary | Phase 3 | 4 |
| Treprostinil Palmitil Inhalation Powder | Lung Diseases, Interstitial | Phase 3 | 4 |
| Treprostinil Palmitil Inhalation Powder | Hypertension | Phase 3 | 3 |
| Treprostinil Palmitil Inhalation Powder | Pulmonary Arterial Hypertension | Phase 3 | 1 |
| ALIS | Mycobacterium Infections, Nontuberculous | Phase 3 | 2 |
Showing 5 of 23 active programs.
Approved assets (10)
Shown in this order: max phase first.
| Drug | Trials |
|---|---|
| Ethambutol | 2 |
| Azithromycin | 2 |
| rhIGF-I/rhIGFBP-3 | 2 |
| Arikayce | 1 |
| Moxifloxacin | 1 |
Showing 5 of 10 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 |
|---|---|
| 67% hit target (n=21) | 40% on time (n=20) |
Journals published in (22)
Shown in this order: most published in first.
| Journal | Publications |
|---|---|
| American journal of respiratory and critical care medicine | 3 |
| Clinical pharmacokinetics | 3 |
| Chest | 2 |
| Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society | 2 |
| Respiratory investigation | 2 |
Showing 5 of 22 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 |
|---|---|---|
| 67 | 18 | 2025-11-25 |
SEC-reported annual financials (11)
Shown in this order: newest fiscal year first; SEC EDGAR XBRL companyfacts, USD as reported.
| Fiscal year | Revenue (USD) | Net income (USD) | R&D (USD) |
|---|---|---|---|
| 2025 | 606,423,000 | -1,276,775,000 | 771,093,000 |
| 2024 | 363,707,000 | -913,772,000 | 598,367,000 |
| 2023 | 305,208,000 | -749,567,000 | 571,011,000 |
| 2022 | 245,358,000 | -481,534,000 | 397,518,000 |
| 2021 | 188,461,000 | -434,654,000 | 272,744,000 |
| 2020 | 164,413,000 | -294,090,000 | 181,157,000 |
| 2019 | 136,467,000 | -254,337,000 | 131,711,000 |
| 2018 | 9,835,000 | -324,277,000 | 145,283,000 |
| 2017 | 0 | -192,649,000 | 109,749,000 |
| 2016 | 0 | -176,273,000 | 122,721,000 |
Showing 10 of 11 fiscal years.
Financing and grant events (40)
Shown in this order: most recent first.
| Date | Round type | Amount (USD) | Source |
|---|---|---|---|
| 2025-06-12 | Follow-on offering | 862,500,000 | Edgar offerings |
| 2025-06-11 | Other financing | not disclosed | Edgar offerings |
| 2025-06-11 | Public offering | 716,300,000 | Sec extracted |
| 2025-06-06 | Debt financing | not disclosed | Sec extracted |
| 2025-04-24 | Debt financing | not disclosed | Sec extracted |
Showing 5 of 40 events.
FDA inspection record (1)
| Latest classification | Inspections |
|---|---|
| NAI | 3 |
Climate targets, as filed (1)
| Reporting year | Net-zero target |
|---|---|
| 2025 | not disclosed |
Workforce and board diversity, as filed (1)
| Reporting year | Workforce % women | Board % women |
|---|---|---|
| 2025 | not disclosed | not disclosed |
Organization relationships (1)
| Related organization | Relationship | Evidence |
|---|---|---|
| Muscular Dystrophy Association | Co sponsors trial with | 1 |
Latest dated events (162)
Shown in this order: newest first.
| Date | Event | Source |
|---|---|---|
| 2026-12-01 | Trial started | Clinical trials (ClinicalTrials.gov) (ClinicalTrials.gov, U.S. National Library of Medicine; AACT database, Clinical Trials Transformation Initiative (CTTI)) |
| 2026-10-29 | Trial started | Clinical trials (ClinicalTrials.gov) (ClinicalTrials.gov, U.S. National Library of Medicine; AACT database, Clinical Trials Transformation Initiative (CTTI)) |
| 2026-08-25 | Trial started | Clinical trials (ClinicalTrials.gov) (ClinicalTrials.gov, U.S. National Library of Medicine; AACT database, Clinical Trials Transformation Initiative (CTTI)) |
| 2026-07-21 | Trial started | Clinical trials (ClinicalTrials.gov) (ClinicalTrials.gov, U.S. National Library of Medicine; AACT database, Clinical Trials Transformation Initiative (CTTI)) |
| 2026-07-20 | Trial started | Clinical trials (ClinicalTrials.gov) (ClinicalTrials.gov, U.S. National Library of Medicine; AACT database, Clinical Trials Transformation Initiative (CTTI)) |
Showing 5 of 162 events.
Biomarker capability evidence (133)
Shown in this order: tier desc, then gene symbol.
| Gene | Role | Evidence |
|---|---|---|
| CCL19 | Trial sponsor | Primary endpoint in a Phase 3 trial |
| INS | Trial sponsor | Named in trial inclusion criteria |
| INS | Trial sponsor | Named in trial inclusion criteria |
| INS | Trial sponsor | Primary endpoint in a Phase 3 trial |
| INS | Trial sponsor | Primary endpoint in a Phase 3 trial |
Showing 5 of 133 evidence rows.
Not on this page
Checked, with nothing recorded for this organization: related companies not grouped here, fda warning letters, fda untitled letters, fda recalls, fda import refusals, manufacturing and distribution sites, clia clinical laboratory certificates, and biomarkers this organization publishes on.