Company profile
TAKEDA PHARMACEUTICAL CO LTD
NYSE:TAKBiotechnology: Pharmaceutical Preparations
Drug pipeline (119)
| Asset | Stage | Revenue | Trials | Status |
|---|---|---|---|---|
| .ALPHA.1-PROTEINASE INHIBITOR HUMAN | approved | — | 6 | approved |
| Alogliptin Benzoate | approved | — | 1 | approved |
| Amoxicillin | approved | — | 14 | approved |
| Amphetamine sulfate | approved | — | 3 | approved |
| ANAGRELIDE HYDROCHLORIDE | approved | — | 2 | approved |
Revenue is the latest reported period from SEC filings. A combination product's amount appears on each of its constituent assets, so those rows are not additive.
Clinical trials (1326)
| NCT ID | Phase | Status | Start | Completion | Sponsor name | Title |
|---|---|---|---|---|---|---|
| NCT03808493 | phase1 | completed | 2019-01-30 | 2019-03-12 | Takeda | A Bioequivalence (BE) Study of TAK-438 Orally Disintegrating (OD) Tablet |
| NCT02401464 | phase1 | completed | 2015-03-01 | 2015-05-01 | Takeda | A Bioequivalence Study of TAK-536 Pediatric Formulation |
| NCT03437564 | phase1 | completed | 2018-02-16 | 2018-04-13 | Takeda | A Bioequivalence Study of the Lu AA21004 20 mg and 2×10 mg Tablets |
| NCT00500149 | phase3 | completed | 2007-06-13 | 2007-12-05 | Shire | A Classroom Study to Assess the Time of Onset of Vyvanse (Lisdexamfetamine Dimesylate) in Pediatric Subjects Aged 6-12 With Attention Deficit/Hyperactivity Disorder (ADHD) |
| NCT03878953 | phase3 | withdrawn | 2022-08-31 | 2023-05-31 | Shire | A Clinical Study of rhPTH(1-84) Treatment in Japanese Participants With Chronic Hypoparathyroidism |
FDA applications (72)
| Application | Type | Applicant | Products | |||
|---|---|---|---|---|---|---|
| BLA 022575 | BLA | Takeda Pharmaceuticals U.S.A., Inc. | ||||
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| BLA 101447 | BLA | Takeda Pharmaceuticals U.S.A., Inc. | ||||
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| BLA 101448 | BLA | Takeda Pharmaceuticals U.S.A., Inc. | ||||
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| BLA 101452 | BLA | Takeda Pharmaceuticals U.S.A., Inc. | ||||
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| BLA 103133 | BLA | Takeda Pharmaceuticals U.S.A., Inc. | ||||
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