SORBITOL

Molecular Excipient

Mwt. LogP HBD HBA PSA RB CSP3
182.0 -3.6 6 6 121.0 5 1.0
CAS
50704
UNII
506T60A25R
SYNONYMS
ZINC ID(s)
Availability
Present in 76 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
NCT00359697 Comparison of Two Different Medications Used to Treat Elevated Intracranial Pressure Phase 1 Not Yet Recruiting
NCT01954290 2015-08-01 Study of Stroke Related Edema Treatments Phase 2 Not Yet Recruiting
NCT02386449 2015-02-01 A Study Comparing Picoprep With Mannitol and Bisacodyl for Colon Cleansing in Preparation for Colonoscopy Phase 4 Recruiting
NCT02306473 2015-01-01 The Leaky Lung Test Phase 0 Not Yet Recruiting
NCT02134353 2014-10-01 A Safety and Efficacy Trial of Inhaled Mannitol in Adult Cystic Fibrosis Subjects Phase 3 Recruiting
NCT02244372 2014-09-01 Efficacy and Safety of Cordyceps Sinensis Mycelium Culture Extract(Paecilomyces Hepiali, CBG-CS-2) on Promotion of Immunity Phase 2/Phase 3 Recruiting
NCT02196142 2014-08-01 Acute Effects of Cortisol on Alcohol Craving in Alcohol Dependence Phase 3 Not Yet Recruiting
NCT02037815 2014-01-01 Correlation of Measured and Calculated Serum Osmolality During Hyperosmolar Drugs Infusion in Patients After Craniotomy Phase 4 Completed
NCT01883531 2013-06-01 Crossover Trial Determining the Efficacy of Dry Powder Mannitol to Improve Lung Function in Subjects Aged 6-17 Years Phase 2 Recruiting
NCT01843088 2013-05-01 Trial of Mannitol Cream for Pain Relief After a Long Run Phase 1 Completed
NCT02091180 2013-01-01 Mannitol Improves Cerebral Oxygen Saturation Phase 4 Completed
NCT01748838 2012-12-01 Phase 1 Study Assessing the Safety and Tolerability of CTX-4430 Phase 1 Completed
NCT01718964 2012-11-01 Acute Effects of Cortisol on Heroin Craving in Opioid Dependence (Ghost-Basel) Phase 2 Completed
NCT01745081 2012-09-01 Comparison of 20% Mannitol and 3% Hypertonic Saline for Cerebral Relaxation During Elective Supratentorial Craniotomies Phase 4 Recruiting
NCT01682408 2012-09-01 Assess Pharmacokinetics of Fostamatinib in Fed and Fasted State in Combination With Ranitidine to Assess Bioavailability Phase 1 Completed
NCT01605357 2012-07-01 Hypernatremia for the Prevention and Treatment of Cerebral Edema in Traumatic Brain Injury Phase 1/Phase 2 Not Yet Recruiting
NCT01645085 2012-07-01 A Study to Assess the Bioequivalence of R406 in Healthy Volunteers When Given 100mg and 150 mg of Fostamatinib Phase 1 Completed
NCT01520207 2012-05-01 Mannitol - Potential Role in Hemodialysis Initiation for Reduction of Intra-dialytic Hypotension Phase 2 Recruiting
NCT01606787 2012-05-01 Mannitol Use During Partial Nephrectomy Prior to Renal Ischemia and Impact on Renal Function Outcomes Phase 3 Recruiting
NCT01485315 2011-11-01 Transfusion-requirements in Septic Shock Trial Phase 3 Completed
NCT01642745 2011-11-01 Mannitol (Aridol) and Methacholine (Provocholine) Responsiveness Phase 4 Completed
NCT01449123 2011-09-01 Mannitol Challenge Test in Adult Asthma Patients With Fixed Dose Combinations Phase 4 Completed
NCT01142505 2010-11-01 Wheeze and Intermittent Treatment Phase 3 Completed
NCT00810940 2010-10-01 Controlled Trial of ABELADRUG200 in Closed, Severe Head Injury Phase 1/Phase 2 Recruiting
NCT01111682 2010-04-01 Hypertonic Saline vs. Mannitol for Elevated Intercranial Pressure Phase 3 Terminated
NCT00669331 2009-11-01 Inhaled Mannitol as a Mucoactive Therapy for Bronchiectasis Phase 3 Completed
NCT00189007 2009-10-01 Antenatal Allopurinol During Fetal Hypoxia Phase 3 Active, Not Recruiting
NCT00973284 2009-09-01 Norwalk Vaccine Study Phase 1/Phase 2 Completed
NCT01309178 2009-05-01 Anti-inflammatory Pulmonal Therapy of Cystic Fibrosis (CF) Patients With Amitriptyline and Placebo Phase 2 Recruiting
NCT01076491 2009-01-01 High Dose Inhaled Mannitol Study Phase 1/Phase 2 Completed
NCT00792714 2008-12-01 Pharmacokinetics of Inhaled Mannitol in Cystic Fibrosis Patients Phase 1 Completed
NCT00795587 2008-10-01 Comparison of 2 Doses of Mannitol on Post Traumatic Intracranial Hypertension and Cerebral Monitoring Phase 4 Terminated
NCT00630812 2008-09-01 Long Term Administration of Inhaled Mannitol in Cystic Fibrosis Phase 3 Completed
NCT00730977 2008-08-01 A Pilot Study to Investigate Administration of Mannitol Via a Novel Dry Powder Inhaler Device Phase 1/Phase 2 Completed
NCT01028339 2008-07-01 Mannitol vs HS to Treat ICHT After Severe TBI : Comparison on PtiO2 and Microdialysis Values Phase 3 Terminated
NCT00569088 2007-11-01 "Study of the Pathogenesis and Molecular Mechanism of ""YURE"" in Internal Intractable Diseases" Phase 2 Recruiting
NCT01233492 2007-10-01 Boron Phenylalanine With or Without Mannitol in Treating Patients With Glioblastoma Multiforme Phase 1 Terminated
NCT00446680 2007-03-01 Long Term Administration of Inhaled Dry Powder Mannitol In Cystic Fibrosis - A Safety and Efficacy Study Phase 3 Completed
NCT00446667 2006-10-01 A Pilot Safety Study of Inhaled Dry Powder Mannitol in Acute Exacerbations of COPD Phase 1/Phase 2 Completed
NCT00446771 2006-10-01 A Pharmacokinetic and Bioavailability Study of Mannitol for Inhalation Using Normal Subjects Phase 1 Completed
NCT00677664 2006-07-01 Effects of Copaxone in the Retinal Function in Diabetic Patients After Panphotocoagulation Phase 4 Active, Not Recruiting
NCT00277537 2006-03-01 Safety and Efficacy of Bronchitol in Bronchiectasis Phase 3 Completed
NCT00117208 2005-11-01 Comparison of Inhaled Mannitol and rhDNase in Children With Cystic Fibrosis Phase 2 Completed
NCT00251056 2005-10-01 Mannitol Dose Response Study in Cystic Fibrosis Phase 2 Completed
NCT00125229 2005-08-01 Cerebral Hemodynamic Effects of Hypertonic Solutions in Severely Head-Injured Patients Phase 4 Terminated
NCT00117182 2005-07-01 Aridol Challenge as a Tool to Predict Treatment Response to Inhaled Corticosteroids in COPD Phase 2 Completed
NCT00238173 2004-12-01 Acetylcysteine, Mannitol, Combination Chemotherapy, and Sodium Thiosulfate in Treating Children With Malignant Brain Tumors Phase 1 Suspended
NCT00113854 2004-10-01 Mannitol as Adjunct Therapy for Childhood Cerebral Malaria Phase 3 Active, Not Recruiting
NCT00455130 2004-03-01 A Phase 2 Study to Determine the Safety and Efficacy of Inhaled Dry Powder Mannitol in Cystic Fibrosis Phase 2 Completed
NCT00319345 2003-11-01 Sodium-Lactate and Traumatic Brain Injury Phase 2/Phase 3 Terminated
NCT00426192 2003-10-01 Effects of Hemofiltration and Mannitol Treatment on Cardiopulmonary-Bypass Induced Immunosuppression Phase 4 Active, Not Recruiting
NCT00390624 2003-07-01 Prevention Of Nephrotoxicity Following Bone Marrow Transplantation Using Urodilatin and Mannitol Phase 2 Completed
NCT00447018 2002-10-01 Mannitol Versus Hypertonic Saline Solution in the Treatment of Elevated Intracranial Pressure Phase 4 Completed

(Browse) Purchasable Analogs in ZINC

Functions of Sorbitol

Misc - Miscellaneous

Regulatory Status of Sorbitol

Gras - Generally recognized as safe.
SORBITOL

Dosages

Route Formulation Per Unit Dose
Buccal Gum, Chewing 212.9MG
Buccal Gum, Chewing 38.1MG
Dental Paste
Intra-Articular Injection 84.83%
Intralesional Injection 45%
Intralesional Injection
Intramuscular Injection 84.83%
Intrasynovial Injection 84.83%
Intravenous Injection 22.5%
Intravenous Injection 7.14%
Intravenous Solution, Injection 48%
Intravenous Solution, Injection 7.14%
Iv(infusion) Injectable 4.7%
Iv(infusion) Injection 56.25%
Iv(infusion) Solution, Injection 35.7%
Iv(infusion) Solution, Injection 7.14%
Nasal Solution 2.5%
Nasal Solution, Spray
Nasal Spray 6.4%
Nasal Spray, Metered 2.86%
Nasal Spray, Metered 6.4%W/V
Ophthalmic Solution 0.2%
Ophthalmic Solution, Drops 0.25%
Ophthalmic Solution, Drops 6.67%
Oral Bar, Chewable
Oral Capsule 185.18MG
Oral Capsule 3.11MG
Oral Capsule, Coated, Soft Gelatin 3.11MG
Oral Capsule, Soft Gelatin 113.6MG
Oral Capsule, Soft Gelatin 28.9MG
Oral Capsule, Soft Gelatin Liquid-Filled
Oral Capsule, Soft Gelatin Liquid-Filled 97MG
Oral Concentrate 40%
Oral Concentrate 60%
Oral Drops 3%
Oral Drops 5%
Oral Granule, For Suspension 28MG
Oral Liquid 5.72%
Oral Liquid 46.4%
Oral Powder, For Suspension 34.28%
Oral Solution 68%
Oral Solution 2GM
Oral Solution, Concentrate 30%
Oral Solution, Elixir 33%
Oral Solution, Elixir 75%
Oral Solution, Liquid 0.01%V/V
Oral Solution, Syrup 50%
Oral Suspension 46%
Oral Suspension 71.4%
Oral Suspension, Drops 25%
Oral Suspension, Liquid 40%
Oral Suspension, Syrup, Sustained Action 2%
Oral Syrup 71.2%
Oral Syrup 50%
Oral Tablet 337.28MG
Oral Tablet 14MG
Oral Tablet (immed./comp. Release), Uncoated, Chewable 316MG
Oral Tablet, Coated 12.96MG
Oral Tablet, Delayed Action, Enteric Coated
Oral Tablet, Extended Release 40.75MG
Oral Tablet, Film Coated 5MG
Oral Tablet, Sustained Action 53.75MG
Rectal Suspension 33.33%
Rectal Suspension 46.18%
Subcutaneous Injectable 4.7%
Subcutaneous Solution, Injection 4.7%
Sublingual Tablet 50.5MG
Topical Cream, Augmented 15%
Topical Emulsion 7%
Topical Emulsion, Cream 5%
Topical Emulsion, Cream 25%
Topical Film, Controlled Release
Topical Lotion
Topical Lotion 5%
Topical Ointment 10%
Topical Ointment 1.5%
Topical Patch 2240MG
Topical Patch, Controlled Release
Topical Solution, Drops 6.9%W/V
Vaginal Emulsion, Cream 36.8%
Vaginal Tablet

More Information

Usage Over Time

Data provided by OpenFDA

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