MEGLUMINE

Molecular Excipient

Mwt. LogP HBD HBA PSA RB CSP3
195.0 -3.4 6 6 113.0 6 1.0
CAS
6284408
UNII
6HG8UB2MUY
SYNONYMS
ZINC ID(s)
Availability
Present in 71 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
NCT00537953 Short Course of Miltefosine and Antimony to Treat Cutaneous Leishmaniasis in Bolivia Phase 2 Recruiting
NCT02233972 2014-08-01 A Drug-Drug Interaction Study To Investigate The Ginkgolides Meglumine Injection To Alter The Pharmacokinetics Of Midazolam Phase 4 Completed
NCT02264535 2014-06-01 A Pilot Study for Ginkgolides Meglumine Injection Skin Testing. Phase 4 Completed
NCT02046031 2014-02-01 Preliminary Study of Pharmacokinetics of Ginkgolides Meglumine Injection. Phase 4 Completed
NCT01953744 2014-01-01 High Dose Fluconazole in Cutaneous Leishmaniasis in Bahia and Manaus Phase 3 Not Yet Recruiting
NCT01958957 2013-06-01 A Safety Study of Ginkgolides Meglumine Injection in the Treatment of Ischemic Stroke. Phase 4 Completed
NCT01806740 2013-03-01 DCE-MRI Using DotaremĀ® in Evaluation of Therapeutic Response to Sorafenib in Patients With Advanced Stage HCC Phase 4 Recruiting
NCT01464242 2011-11-01 Add-on Study of Pentoxifylline in Cutaneous Leishmaniasis Phase 2/Phase 3 Recruiting
NCT01369836 2011-07-01 Study Of Single Doses Of PF-06291826 (Tafamidis) In Japanese And Western Subjects Phase 1 Completed
NCT01050777 2011-03-01 Efficacy of Topical Liposomal Form of Drugs in Cutaneous Leishmaniasis Phase 0 Completed
NCT01211873 2010-09-01 Safety and Efficacy Evaluation of DOTAREMĀ® in MRI of Central Nervous System (CNS) Lesions Phase 3 Completed
NCT00845702 2009-04-01 Renal Magnetic Resonance Angiography (MRA) Study Comparing Dotarem and Time Of Flight (TOF) Phase 3 Terminated
NCT01301924 2008-10-01 Comparison of Low and High Antimonial Dosage in American Cutaneous Leishmaniasis Phase 2/Phase 3 Recruiting
NCT01301937 2008-10-01 Low Antimonial Dosage in American Mucosal Leishmaniasis Phase 2/Phase 3 Recruiting
NCT00818818 2008-08-01 Low-dose Pentavalent Antimony Treatment of Cutaneous Leishmaniasis in Old Age Patients Phase 4 Completed
NCT01032187 2007-10-01 Amphotericin B to Treat Visceral Leishmaniasis in Brazilian Children Phase 4 Completed
NCT00487253 2007-07-01 Oral Miltefosine for the Treatment of Pediatric Cutaneous Leishmaniasis in Colombia Phase 3 Active, Not Recruiting
NCT00600548 2007-07-01 Trial of Miltefosine in Cutaneous Leishmaniasis (Brazil) Phase 2 Completed
NCT00317629 2006-05-01 Controlled Nitric Oxide Releasing Patch Versus Meglumine Antimoniate in the Treatment of Cutaneous Leishmaniasis Phase 3 Terminated
NCT00317980 2006-02-01 Safety and Efficacy of Low-Dose Pentavalent Antimony for Treatment of Cutaneous Leishmaniasis Phase 4 Completed
NCT00973128 2004-02-01 Reduced Doses of Antimony Plus Ranulocyte Monocyte Colony Stimulating Factor (GM-CSF) for Cutaneous Leishmaniasis Phase 2 Completed

(Browse) Purchasable Analogs in ZINC

Dosages

Route Formulation Per Unit Dose
Intra-Arterial Injection
Intra-Articular Injection
Intracardiac Injection
Intradiscal Injection
Intramuscular Injection 15.92%
Intrauterine Injection
Intrauterine Solution
Intravenous Infusion 2.3%
Intravenous Injection 15.92%
Iv(infusion) Injection 7.24%
Oral Capsule, Delayed Action, Enteric Coated
Oral Capsule, Enteric Coated Pellets 3MG
Oral Tablet 24MG
Oral Tablet (immed./comp. Release), Film Coated 1MG
Oral Tablet, Film Coated
Periarticular Injection
Ureteral Solution 7.24%
Urethral Injection
Urethral Solution

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Usage Over Time

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