liothyronine
liothyronine: developed by 1 company · 2 clinical trials tracked · 1 FDA decision.
liothyronine evidence translation
What we can confirm
1 FDA record · 2 tracked trials
What it means
What to watch
Prepared research question
How could liothyronine → RDY affect its developer, and what evidence supports the link?
Traceable citations · Unknowns marked
See linked entities and source evidence1 indications · 1 study sponsors
Related indications
Study sponsors
Development Pipeline (1)
| Company | Phase |
|---|---|
| DR REDDYS LABORATORIES LTD (RDY) | Approved |
Clinical Trials (2)
Thyroid Hormone Replacement After Radio Iodine: Value and Efficacy
Primary endpoint: TSH after two weeks of TH substitution
Phase 2 Study of Intraventricular Omburtamab-based Radioimmunotherapy for Pediatric Patients With Recurrent Medulloblastoma and Ependymoma
Primary endpoint: 2-year event free survival (EFS) in the Recurrent Medulloblastoma Cohort
FDA Decisions1 records
Frequently asked questions
Who is developing liothyronine?
liothyronine is being developed by DR REDDYS LABORATORIES LTD.
How many clinical trials involve liothyronine?
BioSniper tracks 2 clinical trials involving liothyronine.
What is liothyronine's latest FDA decision?
The most recent tracked FDA decision for liothyronine is Approval for 1 INDICATIONS AND USAGE Liothyronine sodium tablets are an L-triiodothyronine (T3) indicated for: Hypothyroidism: As replacement in primary (thyroidal), secondary (pituitary), and tertiary (hypothalamic) congenital or acquired hypothyroidism ( 1.1 ) Pituitary Thyrotropin (Thyroid-Stimulating Hormone, TSH) Suppression: As an adjunct to surgery and radioiodine therapy in the management of well-differentiated thyroid cancer ( 1.2 ) Thyroid Suppression Test: As a diagnostic agent in suppression test, dated March 20, 2009.