NDAORALFOR SOLUTION
Approved
Oct 2006
Lifecycle
LOE Approaching
Competitive Pressure
30/100
Clinical Trials
6
Data completeness
3/8 — Basic
MIRALAX (polyethylene glycol 3350) by Bayer is osmotic activity [moa]. First approved in 2006.
Drug data last refreshed 13h ago · AI intelligence enriched 6d ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
MIRALAX is an oral osmotic laxative containing polyethylene glycol 3350 that draws water into the colon to promote bowel movements. It is used to treat occasional constipation in patients seeking a gentle, non-stimulant option. The drug works through osmotic activity, making it suitable for patients of all ages including children.
LOE Approaching
Product is in late-stage lifecycle with 30% competitive pressure, signaling a smaller, defensive marketing team focused on market maintenance rather than growth expansion.
Mechanism of Action
Osmotic Activity
Pharmacologic Class:
Osmotic Laxative
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Clinical Trials (6)
To Evaluate Patient Preference of Movantik and Polyethylene Glycol 3350 for Opioid Induced Constipation
Started Mar 2017
276 enrolled
Opioid Induced Constipation
Efficacy and Safety of Polyethylene Glycol 3350 (PEG 3350) for Relief of Constipation (MK-8114-005)
Started Dec 2015
0Constipation
Study to Investigate Prucalopride vs. Polyethylene Glycol 3350 on Colon Activity
Started Feb 2013
13 enrolled
Chronic Constipation
Dose-Finding Trial of Polyethylene Glycol 3350 Laxative Plus Electrolytes for the Treatment of Constipation (Protocol P07515)
Started Oct 2010
154 enrolled
Constipation
Miralax (PEG 3350) vs. Golytely as Bowel Preparation for Screening Colonoscopy
Started Apr 2010
136 enrolled
Colon Cancer
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Data Sources
- Drug label: DailyMed / FDA
- Clinical trials: ClinicalTrials.gov
- Patent data: FDA Orange Book
- Spending data: CMS Medicare
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.