Last Updated: May 22, 2026

CLINICAL TRIALS PROFILE FOR NUVARING


✉ Email this page to a colleague

« Back to Dashboard


All Clinical Trials for NUVARING

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00269620 ↗ PARIS or PAtch RIng Study: A Trial to Evaluate NuvaRing Versus OrthoEvra Completed Magee-Womens Hospital Phase 4 2005-06-01 This is an open-label prospective, multicenter, randomized trial to compare continuation rates into the fourth cycle of women using either the NuvaRing or OrthoEvra. Five hundred women will be recruited at 9 centers nationwide to be randomly assigned to use either the NuvaRing or OrthoEvra for four months. Women must either be on the pill or have recently stopped the pill and be relatively satisfied with oral contraceptive use to qualify for enrollment. Two visits and two phone calls will be required.
NCT00269620 ↗ PARIS or PAtch RIng Study: A Trial to Evaluate NuvaRing Versus OrthoEvra Completed Organon Phase 4 2005-06-01 This is an open-label prospective, multicenter, randomized trial to compare continuation rates into the fourth cycle of women using either the NuvaRing or OrthoEvra. Five hundred women will be recruited at 9 centers nationwide to be randomly assigned to use either the NuvaRing or OrthoEvra for four months. Women must either be on the pill or have recently stopped the pill and be relatively satisfied with oral contraceptive use to qualify for enrollment. Two visits and two phone calls will be required.
NCT00269620 ↗ PARIS or PAtch RIng Study: A Trial to Evaluate NuvaRing Versus OrthoEvra Completed University of Pittsburgh Phase 4 2005-06-01 This is an open-label prospective, multicenter, randomized trial to compare continuation rates into the fourth cycle of women using either the NuvaRing or OrthoEvra. Five hundred women will be recruited at 9 centers nationwide to be randomly assigned to use either the NuvaRing or OrthoEvra for four months. Women must either be on the pill or have recently stopped the pill and be relatively satisfied with oral contraceptive use to qualify for enrollment. Two visits and two phone calls will be required.
NCT00357526 ↗ Oral Contraceptive Pills Compared to Vaginal Rings Completed Organon N/A 2003-04-01 The purpose of this study is to determine whether teens and young women would prefer the Nuvaring to oral contraceptive pills after having tried both methods.
NCT00357526 ↗ Oral Contraceptive Pills Compared to Vaginal Rings Completed University of California, San Francisco N/A 2003-04-01 The purpose of this study is to determine whether teens and young women would prefer the Nuvaring to oral contraceptive pills after having tried both methods.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for NUVARING

Condition Name

Condition Name for NUVARING
Intervention Trials
Contraception 6
Bacterial Vaginosis 2
Infertility 2
HIV 2
[disabled in preview] 1
This preview shows a limited data set
Subscribe for full access, or try a Trial

Condition MeSH

Condition MeSH for NUVARING
Intervention Trials
Vaginosis, Bacterial 3
Infertility 2
Polycystic Ovary Syndrome 2
Vaginal Diseases 2
[disabled in preview] 1
This preview shows a limited data set
Subscribe for full access, or try a Trial

Clinical Trial Locations for NUVARING

Trials by Country

Trials by Country for NUVARING
Location Trials
United States 28
Thailand 2
Canada 2
Peru 2
South Africa 2
This preview shows a limited data set
Subscribe for full access, or try a Trial

Trials by US State

Trials by US State for NUVARING
Location Trials
Virginia 3
New York 3
Illinois 3
California 3
Pennsylvania 2
This preview shows a limited data set
Subscribe for full access, or try a Trial

Clinical Trial Progress for NUVARING

Clinical Trial Phase

Clinical Trial Phase for NUVARING
Clinical Trial Phase Trials
Phase 4 11
Phase 3 2
Phase 2 3
[disabled in preview] 11
This preview shows a limited data set
Subscribe for full access, or try a Trial

Clinical Trial Status

Clinical Trial Status for NUVARING
Clinical Trial Phase Trials
Completed 17
Unknown status 4
Terminated 3
[disabled in preview] 3
This preview shows a limited data set
Subscribe for full access, or try a Trial

Clinical Trial Sponsors for NUVARING

Sponsor Name

Sponsor Name for NUVARING
Sponsor Trials
Merck Sharp & Dohme Corp. 8
Organon 4
National Institute of Allergy and Infectious Diseases (NIAID) 2
[disabled in preview] 4
This preview shows a limited data set
Subscribe for full access, or try a Trial

Sponsor Type

Sponsor Type for NUVARING
Sponsor Trials
Other 26
Industry 17
NIH 3
[disabled in preview] 1
This preview shows a limited data set
Subscribe for full access, or try a Trial
Last updated: April 28, 2026

NuvaRing (etonogestrel/ethinyl estradiol vaginal ring): Clinical-Development Update and Market Outlook

What is NuvaRing and what is the current clinical development footprint?

NuvaRing is a combined hormonal contraceptive (CHC) delivered as a flexible vaginal ring releasing etonogestrel (ENG) and ethinyl estradiol (EE). It is an established, marketed product with long-standing clinical use; no broad, regulator-signaled late-stage “new indication” program is publicly documented in the routine trial registries as a dominant driver of near-term expansion.

Across publicly accessible trial registries, NuvaRing’s clinical activity is dominated by:

  • Label maintenance / post-marketing surveillance
  • Pharmacokinetic (PK) and formulation comparison studies
  • Contraceptive effectiveness and safety observations that support continued marketing

Implication for investors and R&D leaders: the drug’s value proposition today is anchored in market share, persistence, and payer access, not in a visible pipeline that would materially reset timelines or add a new regulatory exclusivity layer.


What does the trial landscape show by study type and likely intent?

Publicly visible NuvaRing-related clinical activity tends to cluster into four buckets:

Study type Typical endpoints Typical sponsor intent Commercial impact
PK / bioequivalence Serum ENG/EE AUC, Cmax, time profile Support manufacturing scale-up, generic/authorized-brand lifecycle Low incremental innovation value
Safety and tolerability Adverse event rates, bleeding pattern Maintain label and manage risk programs Sustains formulary positioning
Contraceptive efficacy studies Pregnancy rates, cycle-to-cycle effectiveness Confirm real-world performance and adherence effect Sustains payer and prescriber confidence
Special population studies Adolescents, switching from OCP, etc. Broaden usability within existing indication Moderate effect on penetration

Sources for NuvaRing composition, indication, and clinical use framework are FDA-reviewed labeling materials and professional product monographs. FDA label is the baseline reference for dosing and safety endpoints. See NuvaRing label. [1]


How large is the NuvaRing opportunity in the contraception market?

Where does NuvaRing sit in the contraception portfolio?

NuvaRing competes within the CHC class, alongside:

  • Oral contraceptive pills (daily CHCs)
  • Transdermal patches (e.g., norelgestromin/EE)
  • Long-acting reversible contraception (LARC) such as IUDs and implants (competes indirectly)

The core competitive lever for NuvaRing is user adherence. Compared with daily OCPs, the ring provides dosing periodicity aligned to a monthly cycle; compared with patches, it offers a different comfort and adherence profile.


What is the market structure and how does it drive pricing power?

In CHC contraception, pricing pressure is the norm due to:

  • Broad genericization of ethinyl estradiol plus progestins across OCPs
  • Class-level competition that shifts demand based on coverage rules and copays
  • Channel mix (retail vs mail order) that tends to reward lowest net cost for payers

That structure typically limits the magnitude of pricing upside for established brand CHCs, unless:

  • A product has meaningful formulary differentiation (inclusion tiering)
  • A brand maintains supply continuity and consistent net pricing
  • Switch costs or patient preference remain strong in a protected niche

NuvaRing’s market reality: the product competes in a mature class where incremental share gains come more from coverage and patient persistence than from breakthrough clinical differentiation.


Market analysis and projection

What demand drivers likely matter most for NuvaRing (2026–2030)?

Contraception demand depends on population and behavior, but NuvaRing growth or decline in any geography is usually governed by:

  1. Formulary access
    • Preferred-tier placement drives higher conversion from prescriptions
  2. Adherence and persistence
    • Switching off CHCs is common; ring-specific satisfaction can slow churn
  3. Safety perception
    • Clinician comfort and patient risk tolerance affect uptake
  4. Channel competition
    • Mail order pricing and plan designs shift relative economics versus OCPs
  5. Supply and continuity
    • Any disruption can cause lost loyalty due to adherence behavior

This is consistent with CHC commercial dynamics described in regulatory and public health materials that emphasize real-world adherence and counseling. [2]


Market projection framework (scenario-based, class-level constrained)

Because NuvaRing is not currently supported by a clearly visible late-stage, label-expanding development program in public trial registries, projection should be treated as a mature-product trajectory dominated by share, churn, and payer dynamics.

A practical projection model for 2026–2030 uses:

  • Base population growth (incremental users)
  • CHC share vs LARC share (structural)
  • Within-CHC switch rates (ring vs pill vs patch)
  • Price and net-to-gross evolution (formulary pressure)

Most likely outcome for a mature CHC like NuvaRing: modest volume growth where coverage is stable, offset by pricing pressure where generic OCPs dominate formulary cost controls.


What do the latest public artifacts imply for near-term upside?

NuvaRing’s latest publicly accessible artifacts are consistent with a product that remains in routine clinical practice and labeling. The FDA label provides established dosing instructions and safety warnings that sustain clinician familiarity. [1]

If any future upside emerges, it is typically tied to:

  • payer renegotiations that improve net position
  • improved access in state and commercial plan formularies
  • population shifts among CHC users who prefer non-oral delivery

Competitive positioning

How does NuvaRing compare to main CHC delivery alternatives?

Attribute NuvaRing (vaginal ring) OCP CHCs Transdermal patch CHCs
Dosing frequency Monthly ring replacement Daily Weekly
Adherence mechanism Reduced daily action Requires daily adherence Requires weekly changes
Market pressure Mature, class-generic dynamics High generic penetration Less generic competition than OCPs
Key risk messaging CHC class VTE risk counseling Same class risk counseling Same class risk counseling

This comparison reflects the common clinical and utilization differences among CHC delivery forms and the shared CHC safety counseling framework. [1][2]


What is the patent and exclusivity relevance for business strategy?

For established marketed products, patent strategy typically focuses on:

  • Formulation/manufacturing improvements
  • Method-of-use niches
  • Landscape around authorized generics and licensing

However, without a specific, current patent-expiration map for NuvaRing across target jurisdictions in the materials provided here, the actionable planning should be based on clinical and market realities: mature product behavior, payer economics, and competitive churn rather than pipeline-led step changes.


Key Takeaways

  • NuvaRing is a mature CHC with clinical activity centered on maintenance-type studies rather than a visible, label-expanding late-stage program in public registries.
  • Near-term value is driven by market access and persistence more than by clinical breakthroughs.
  • 2026–2030 upside is likely modest and constrained by CHC generic pricing dynamics, unless payer placement materially improves.
  • Projection should model churn and formulary tiering as first-order variables, with population growth as a secondary driver.

FAQs

1) Is NuvaRing still actively studied in clinical trials?

Yes, but the visible activity is mostly consistent with post-marketing or support studies (PK, safety, and effectiveness maintenance) rather than a dominant late-stage expansion program. [1]

2) What are the active ingredients in NuvaRing?

NuvaRing contains etonogestrel and ethinyl estradiol delivered via a vaginal ring. [1]

3) Does NuvaRing have the same core safety counseling as other CHCs?

Yes. As a CHC, it carries the class-level counseling themes around bleeding patterns and thromboembolic risk consistent with CHC labeling. [1]

4) What is the main commercial threat to NuvaRing?

Pricing and formulary pressure from competing CHC options, especially generic oral contraceptives, combined with switching behavior among users. [2]

5) What is the strongest lever for growth?

Improved formulary placement and net pricing stability that improves conversion and reduces churn relative to pill and patch CHCs. [2]


References

[1] U.S. Food and Drug Administration. NuvaRing (etonogestrel/ethinyl estradiol) prescribing information and labeling. FDA.
[2] Centers for Disease Control and Prevention. U.S. Medical Eligibility Criteria for Contraceptive Use (CHC guidance and counseling considerations). CDC.

More… ↓

⤷  Start Trial

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.