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 |