NDAINTRAUTERINESYSTEM1 Generic Approved
Approved
Jan 2013
Lifecycle
Peak
Competitive Pressure
23/100
Clinical Trials
20
Data completeness
5/8 — Partial
SKYLA (levonorgestrel) by Bayer. Approved for progestin [epc]. First approved in 2013.
Drug data last refreshed 11h ago · AI intelligence enriched 14h ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
SKYLA is a subdermal intrauterine levonorgestrel-releasing system approved in 2013 for contraception. It releases a synthetic progestin directly into the uterus to prevent pregnancy through multiple mechanisms including cervical mucus thickening and endometrial suppression. SKYLA is a small-molecule hormone delivery device positioned as a lower-dose alternative to other levonorgestrel IUDs.
$0.013BPart D
Peak3.0 years to LOESKYLA is in peak lifecycle but faces significant intra-Bayer cannibalization; limited growth trajectory suggests smaller, specialized commercial team focus.
Mechanism of Action
Pharmacologic Class:
Progestin
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Clinical Trials (20)
Effects of Copper Versus Levonorgestrel Intrauterine Devices on Mucosal Microbiota and Barrier Function Among Young African Women
Started Jul 2026
120 enrolled
Vaginal Microbial Diversity
Evaluate the Effect of Vimseltinib on Pharmacokinetics of Combined Oral Contraceptive (Ethinyl Estradiol/Levonorgestrel)
Started Jun 2026
24 enrolled
Healthy Participants
A Study to Evaluate the Efficacy and Safety of Subcutaneous Levonorgestrel Butanoate for Female Contraception
Started Apr 2026
165 enrolled
Healthy WomenFemale Contraception
A Phase 1 Study to Assess the Effect of ABBV-722 on Ethinyl Estradiol and Levonorgestrel Drug Levels in Healthy Adult Female Participants
Started Mar 2026
15 enrolled
Healthy Volunteer
Drug-drug Interaction Study of Bemnifosbuvir/Ruzasvir (BEM/RZR) and Ethinyl Estradiol/Levonorgestrel (EE/LNG)
Started Dec 2025
24 enrolled
Healthy Volunteer Study
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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.