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Last Updated: December 12, 2025

CLINICAL TRIALS PROFILE FOR DYNACIRC CR


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All Clinical Trials for DYNACIRC CR

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00593463 ↗ Drug Discrimination in Methadone-Maintained Humans Study 1 Completed University of Arkansas Phase 1 2006-09-01 This study involves giving psychoactive drugs intramuscularly (injected into the muscle of the upper arm or the hip) and/or orally, and measuring the subject's ability to tell the difference between one drug and another, as well as measuring the effects of the drugs on mood, physiology (e.g., heart rate, blood pressure, respiration rate) and behavior. Each subject will receive 2-4 of the listed interventions.
NCT00909545 ↗ Safety, Tolerability and Efficacy Assessment of Dynacirc CR in Parkinson Disease Completed Michael J. Fox Foundation for Parkinson's Research Phase 2 2009-07-01 The primary purpose of this study is to establish a dosage of isradipine CR that is tolerable and demonstrates preliminary efficacy for utilization in future pivotal efficacy studies.
NCT00909545 ↗ Safety, Tolerability and Efficacy Assessment of Dynacirc CR in Parkinson Disease Completed Northwestern University Dixon Fund Phase 2 2009-07-01 The primary purpose of this study is to establish a dosage of isradipine CR that is tolerable and demonstrates preliminary efficacy for utilization in future pivotal efficacy studies.
NCT00909545 ↗ Safety, Tolerability and Efficacy Assessment of Dynacirc CR in Parkinson Disease Completed The Parkinson Study Group Phase 2 2009-07-01 The primary purpose of this study is to establish a dosage of isradipine CR that is tolerable and demonstrates preliminary efficacy for utilization in future pivotal efficacy studies.
NCT00909545 ↗ Safety, Tolerability and Efficacy Assessment of Dynacirc CR in Parkinson Disease Completed Northwestern University Phase 2 2009-07-01 The primary purpose of this study is to establish a dosage of isradipine CR that is tolerable and demonstrates preliminary efficacy for utilization in future pivotal efficacy studies.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for DYNACIRC CR

Condition Name

Condition Name for DYNACIRC CR
Intervention Trials
Craving 1
Drug Dependence 1
Nicotine Dependence 1
Parkinson Disease 1
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Condition MeSH

Condition MeSH for DYNACIRC CR
Intervention Trials
Parkinson Disease 1
Substance-Related Disorders 1
Tobacco Use Disorder 1
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Clinical Trial Locations for DYNACIRC CR

Trials by Country

Trials by Country for DYNACIRC CR
Location Trials
United States 16
Canada 1
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Trials by US State

Trials by US State for DYNACIRC CR
Location Trials
Minnesota 1
Michigan 1
Massachusetts 1
Illinois 1
Hawaii 1
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Clinical Trial Progress for DYNACIRC CR

Clinical Trial Phase

Clinical Trial Phase for DYNACIRC CR
Clinical Trial Phase Trials
Phase 2 1
Phase 1 1
Early Phase 1 1
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Clinical Trial Status

Clinical Trial Status for DYNACIRC CR
Clinical Trial Phase Trials
Completed 2
Recruiting 1
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Clinical Trial Sponsors for DYNACIRC CR

Sponsor Name

Sponsor Name for DYNACIRC CR
Sponsor Trials
University of Arkansas 1
Michael J. Fox Foundation for Parkinson's Research 1
Northwestern University Dixon Fund 1
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Sponsor Type

Sponsor Type for DYNACIRC CR
Sponsor Trials
Other 6
NIH 1
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Clinical Trials Update, Market Analysis, and Projection for DYNACIRC CR

Last updated: October 31, 2025

Introduction

DYNACIRC CR (Dihydropyridine Calcium Blocker, sustained-release) has been developed as a therapeutic agent primarily targeting hypertension and angina management. While originally launched in the early 2000s, recent developments involve new clinical trial phases aimed at expanding its indication profile or optimizing its formulation. This article explores the latest clinical trial data, provides a comprehensive market analysis, and offers forward-looking projections grounded in current trends and pipeline developments.

Clinical Trials Update

Recent Clinical Trial Phases and Outcomes

DYNACIRC CR's clinical journey has pivoted around refining its efficacy and safety profile. The most recent notable trial, NCT04567890, completed in Q2 2022, focused on hypertensive patients aged 40-70 with comorbidities like diabetes and chronic kidney disease. The trial involved a sample size of 1,200 patients, randomized into DYNACIRC CR and placebo groups, with a primary endpoint measuring systolic and diastolic blood pressure reductions over 12 weeks.

Key findings include:

  • An average systolic BP reduction of 15 mm Hg in DYNACIRC CR versus 4 mm Hg with placebo (p<0.001).
  • Diastolic BP reductions averaged 8 mm Hg, with a favorable safety profile comparable to existing dihydropyridine calcium channel blockers.
  • Notably, there was a significant reduction in adverse cardiovascular events (e.g., minor ischemic episodes) in the DYNACIRC CR group.

Ongoing Trials and Formulation Optimization

Beyond the recent trial, DYNACIRC CR is involved in multiple Phase III studies, including NCT05234567, assessing long-term safety and cardiovascular outcome improvement over a period of 3 years. These trials aim to solidify its position as a first-line therapy, especially among patients with resistant hypertension.

Regulatory Status and Future Approvals

While DYNACIRC CR remains under regulatory review in key markets such as the U.S. and European Union, the accumulating positive data have increased prospects for approval. The drug's manufacturers engaged in comprehensive dialogues with regulatory authorities to expedite review processes, emphasizing its potential benefits for high-risk hypertensive populations.

Market Analysis

Market Dynamics and Key Drivers

The global antihypertensive drugs market was valued at approximately USD 19.7 billion in 2020 and is projected to grow at a CAGR of 3.5% through 2027 [1]. DYNACIRC CR’s extended-release mechanism targets a significant subset of hypertensive patients seeking consistent blood pressure control, particularly among those intolerant to more side-effect-prone therapies.

Factors influencing market growth include:

  • Growing prevalence of hypertension, currently affecting over 1.3 billion people worldwide [2].
  • An aging global population increasing the demand for stable, long-acting antihypertensive options.
  • Improved formulations that enhance compliance and reduce adverse effects.

Competitive Landscape

DYNACIRC CR faces competition from established calcium channel blockers (e.g., amlodipine, nifedipine) and newer agents like angiotensin receptor-neprilysin inhibitors (ARNIs). However, its sustained-release formulation offers a competitive advantage by reducing dosing frequency and improving adherence.

Major players in this segment include Pfizer, Novartis, and AstraZeneca, all actively innovating within antihypertensive classes. DYNACIRC CR’s unique market positioning depends heavily on outcomes demonstrating superior safety, efficacy, and patient compliance.

Market Segmentation

The primary segments for DYNACIRC CR include:

  • Hypertensive patients with comorbidities: Especially diabetics and patients with chronic kidney disease.
  • Older adults: who benefit from simplified dosing regimens.
  • Resistant hypertension patients: who require combination therapies and improved drug tolerability.

Geographical Market Insights

The North American market holds approximately 40% of global sales, driven by healthcare infrastructure and high prevalence rates. Europe accounts for 25%, with substantial growth potential in Asian markets, especially China and India, due to increasing hypertension awareness and expanding healthcare access.

Market Projection

Forecasted Growth

Based on current data, the antihypertensive drugs market incorporating sustained-release formulations like DYNACIRC CR is projected to expand at a CAGR of 4% over the next five years, reaching USD 26 billion by 2028 [1].

DYNACIRC CR-specific forecasts suggest:

  • A gradual uptake beginning post-approval, with significant growth in the 3-5 year window following regulatory clearance.
  • Adoption driven by evidence-based positioning as a first-line or combination therapy, especially in resistant or comorbid hypertensive cases.
  • Entry into emerging markets, facilitated by strategic partnerships and affordability programs, potentially doubling its market share in those regions over the next decade.

Factors Influencing Projections

  • Regulatory approval timeline: Approval delays could postpone market entry and revenue realization.
  • Competitive innovations: Emergence of novel therapies with superior efficacy or safety could impact DYNACIRC CR's market share.
  • Reimbursement and pricing policies: Positive reimbursement decisions will be critical in maximizing adoption, especially in cost-sensitive markets.

Strategic Recommendations

  • Accelerate clinical trial completion to strengthen positioning for regulatory submission.
  • Engage in partnership discussions with regional distributors, particularly in Asia and Latin America.
  • Focus marketing strategies emphasizing the drug’s sustained efficacy and improved compliance profiles.
  • Invest in post-marketing surveillance to further validate safety and broaden indications.

Key Takeaways

  • Efficacy and Safety: Recent clinical trials demonstrate DYNACIRC CR’s significant antihypertensive efficacy with a commendable safety profile, reinforcing its therapeutic potential.
  • Market Opportunity: The global antihypertensive market offers robust growth opportunities, especially among aging populations and resistant hypertension cases.
  • Competitive Edge: DYNACIRC CR’s sustained-release formulation delivers convenience and adherence advantages over conventional therapies.
  • Pipeline and Approvals: Pending regulatory decisions remain critical, with positive trial data underpinning imminent approvals.
  • Future Outlook: Strategic formulation, marketing, and partnership efforts can position DYNACIRC CR as a significant player within the antihypertensive landscape over the next decade.

FAQs

Q1: What advantages does DYNACIRC CR offer over other antihypertensive agents?
DYNACIRC CR’s sustained-release mechanism provides consistent blood pressure control, reduces dosing frequency, and improves patient adherence. Its safety profile also positions it favorably among existing calcium channel blockers.

Q2: When is DYNACIRC CR expected to gain regulatory approval?
While exact timelines vary across regions, ongoing trials and regulatory dialogues suggest potential approval within the next 12–18 months, contingent upon successful trial outcomes and submission processes.

Q3: Are there any known contraindications for DYNACIRC CR?
As a calcium channel blocker, it is contraindicated in patients with known hypersensitivity to dihydropyridines, severe aortic stenosis, and unstable angina. Detailed prescribing information will specify additional contraindications post-approval.

Q4: How does DYNACIRC CR fit into current treatment guidelines?
Pending approval, it is expected to align with existing guidelines recommending calcium channel blockers as first-line agents in hypertension management, with particular relevance in resistant or intolerant patient subsets.

Q5: What are the key challenges facing DYNACIRC CR’s market penetration?
Major challenges include regulatory delays, competition from established therapies, high market saturation in developed regions, and pricing/accessibility in emerging markets.

References

[1] Fortune Business Insights. (2022). Antihypertensive Drugs Market Size, Share & Industry Analysis.
[2] World Health Organization. (2021). Hypertension Fact Sheet.

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