DIETHANOLAMINE

Molecular Excipient

Mwt. LogP HBD HBA PSA RB CSP3
105.0 -1.4 3 3 52.0 4 1.0
CAS
111422
UNII
AZE05TDV2V
SYNONYMS
ZINC ID(s)
Availability
Present in 57 ZINC catalogs

Known Active Genes

There has not been any activity reported at 10μM or less for this excipient (per ChEBML)

Clinical Trials

This compound has been an intervention in the following clincial trials (per clinicaltrials.gov).
Code Date Title Phase Status
NCT01934582 2013-08-01 A Pharmacokinetic Substudy of the TDE-PH-304 Protocol Phase 3 Active, Not Recruiting
NCT01560624 2012-07-01 Trial of the Early Combination of Oral Treprostinil With Background Oral Monotherapy in Subjects With Pulmonary Arterial Hypertension Phase 3 Recruiting
NCT01560637 2012-05-01 An Open-Label, Long-Term Study of Oral Treprostinil in Subjects With Pulmonary Arterial Hypertension Phase 3 Recruiting
NCT01172496 2010-08-01 A Bioavailability Study Comparing Treprostinil Diethanolamine Oral Tablets and Oral Solution in Healthy Volunteers Phase 1 Completed
NCT01153386 2010-07-01 Pharmacokinetic Linearity and Comparative Bioavailability of Treprostinil Diethanolamine Phase 1 Completed
NCT01165476 2010-07-01 Comparative Bioavailability of Treprostinil Diethanolamine Manufactured by Two Independent Facilities Phase 1 Completed
NCT01131845 2010-05-01 The Effect of Renal Impairment on the Pharmacokinetics of Oral Treprostinil Phase 1 Completed
NCT00963001 2009-09-01 Effect of Food on the Pharmacokinetics of Oral Treprostinil Phase 1 Completed
NCT00963027 2009-09-01 Effect of Esomeprazole on the Pharmacokinetics of Oral Treprostinil Phase 1 Completed
NCT00848107 2009-09-01 Open-Label Study of Oral Treprostinil in Digital Ulcers Phase 2 Terminated
NCT00775463 2009-05-01 Digital Ischemic Lesions in Scleroderma Treated With Oral Treprostinil Diethanolamine Phase 2 Completed
NCT00848939 2008-12-01 Pharmacokinetics of Oral Treprostinil in Patients With Systemic Sclerosis Phase 1 Completed
NCT00445159 2006-11-01 UT-15C SR in the Treatment of Critical Limb Ischemia Phase 2 Recruiting
NCT01027949 2006-05-01 An Open-Label Extension Trial of UT-15C SR in Subjects With Pulmonary Arterial Hypertension Phase 3 Active, Not Recruiting

(Browse) Purchasable Analogs in ZINC

Dosages

Route Formulation Per Unit Dose
Iv(infusion) Injection 1.5%
Ophthalmic Solution
Topical Emulsion, Cream 0.3%

More Information

Usage Over Time

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