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Last Updated: November 12, 2025

CLINICAL TRIALS PROFILE FOR VECURONIUM BROMIDE


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All Clinical Trials for Vecuronium Bromide

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00970762 ↗ Comparative Study of Rocuronium With Vecuronium (Study 71101)(COMPLETED) Completed Merck Sharp & Dohme Corp. Phase 3 2003-02-01 This study was conducted to determine and compare the safety and effectiveness of two neuromuscular blockers (rocuronium and vecuronium) at various doses in adults who are undergoing general elective surgery with sevoflurane anesthesia. Study participants received an intubating dose of a neuromuscular blocker (to enable insertion of a tube through the nose or mouth into the trachea to provide artificial ventilation). The intubating dose was followed by repeated bolus maintenance doses as needed, to maintain muscle relaxation. The time it takes to reach maximal effect of the neuromuscular blocker (onset time) after the intubating dose was measured and compared as the primary outcome.
NCT01116713 ↗ Effect of Dexamethasone in Postoperative Symptoms After Mastectomy for Breast Cancer Completed Instituto Mexicano del Seguro Social Phase 3 2009-06-01 Postoperative pain, nausea and vomiting (PONV) are the most common complications after anesthesia and surgery. Women undergoing mastectomy with axillary dissection are at a particularly high risk for the development of PONV and an incidence of 60-80% in patients receiving no antiemetic has been reported. Emetic episodes predispose to aspiration of gastric contents, wound dehiscence, psychological distress, and delayed recovery and discharge times. These justify the use of prophylactic antiemetics in women scheduled for mastectomy. Most of the currently used antiemetics, including antihistamines, butyrophenones and dopamine receptor antagonists have been reported to cause occasional undesirable adverse effects, such as excessive sedation, hypotension, dry mouth, dysphoria, hallucinations and extrapyramidal signs. Antiserotonins (e.g., ondansetron) are available for the prevention and treatment of PONV in patients undergoing various types of surgery [4]. However, the use of prophylactic antiemetic therapy with antiserotonins has been criticized for being too expensive. Dexamethasone was first reported to be an effective antiemetic regimen in patients receiving cancer chemotherapy. The purpose of this study was to evaluate the efficacy of dexamethasone treatment for reducing pain and PONV as well as analgesic and antiemetic requirements in women undergoing general anesthesia for mastectomy with axillary lymph node dissection.
NCT01690338 ↗ A Study of Residual Curarization Incidence in China Unknown status Central South University Phase 4 2012-10-01 The purpose of this study is to determine the incidence of residual curarization in PACU and relevant risk factors.
NCT01690338 ↗ A Study of Residual Curarization Incidence in China Unknown status China Medical University Hospital Phase 4 2012-10-01 The purpose of this study is to determine the incidence of residual curarization in PACU and relevant risk factors.
NCT01690338 ↗ A Study of Residual Curarization Incidence in China Unknown status Chinese PLA General Hospital Phase 4 2012-10-01 The purpose of this study is to determine the incidence of residual curarization in PACU and relevant risk factors.
NCT01690338 ↗ A Study of Residual Curarization Incidence in China Unknown status Eastern Hepatobiliary Surgery Hospital Phase 4 2012-10-01 The purpose of this study is to determine the incidence of residual curarization in PACU and relevant risk factors.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for Vecuronium Bromide

Condition Name

Condition Name for Vecuronium Bromide
Intervention Trials
Anesthesia 4
Reversal of Neuromuscular Blockade 3
Residual Neuromuscular Block 2
Neuromuscular Blocking Agents 2
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Condition MeSH

Condition MeSH for Vecuronium Bromide
Intervention Trials
Delayed Emergence from Anesthesia 3
Hepatoblastoma 1
Breast Neoplasms 1
Syndrome 1
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Clinical Trial Locations for Vecuronium Bromide

Trials by Country

Trials by Country for Vecuronium Bromide
Location Trials
United States 30
China 13
Austria 3
India 2
Germany 2
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Trials by US State

Trials by US State for Vecuronium Bromide
Location Trials
Wisconsin 2
Texas 2
Tennessee 2
Pennsylvania 2
Ohio 2
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Clinical Trial Progress for Vecuronium Bromide

Clinical Trial Phase

Clinical Trial Phase for Vecuronium Bromide
Clinical Trial Phase Trials
PHASE4 2
Phase 4 8
Phase 3 2
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Clinical Trial Status

Clinical Trial Status for Vecuronium Bromide
Clinical Trial Phase Trials
Completed 7
Unknown status 4
NOT_YET_RECRUITING 2
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Clinical Trial Sponsors for Vecuronium Bromide

Sponsor Name

Sponsor Name for Vecuronium Bromide
Sponsor Trials
Merck Sharp & Dohme Corp. 3
Wuhan Union Hospital, China 2
The First Affiliated Hospital of Zhengzhou University 2
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Sponsor Type

Sponsor Type for Vecuronium Bromide
Sponsor Trials
Other 47
Industry 3
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Clinical Trials Update, Market Analysis, and Projection for Vecuronium Bromide

Last updated: October 27, 2025

Introduction

Vecuronium bromide stands as a prominent neuromuscular blocking agent widely utilized in anesthesia during surgical procedures and intensive care settings. As a non-depolarizing muscle relaxant, vecuronium facilitates endotracheal intubation and surgical muscle relaxation, with favorable pharmacokinetic properties such as predictable onset and recovery times. Its safety and efficacy profiles continue to propel research, influence market dynamics, and shape investment strategies within the pharmaceutical and healthcare sectors.

This article offers a comprehensive update on ongoing and completed clinical trials, evaluates the current market landscape, and provides future projections for vecuronium bromide, equipping stakeholders with critical insights for strategic decision-making.


Clinical Trials Update

Current Landscape of Clinical Research

Recent years have seen limited novel clinical trials specifically targeting vecuronium bromide, primarily due to its well-established profile in clinical practice. However, ongoing research focuses on optimizing delivery mechanisms, exploring combination therapies, and evaluating safety profiles in special patient populations.

  • Phase IV Post-Marketing Surveillance: The majority of ongoing studies are observational, monitoring long-term safety and rare adverse events in diverse patient demographics. These are primarily sponsored by hospital networks and academic institutions aiming to refine dosing protocols and adverse effect management.

  • Innovative Delivery Systems: Recent trials investigate alternative administration routes, such as transdermal or inhalational delivery, to enhance convenience and patient compliance, though these remain in early phases.

  • Safety and Efficacy in Pediatric and Geriatric Populations: Trials are underway assessing dosing adjustments and safety, addressing unmet clinical needs in vulnerable groups.

Notable Completed Trials

While large-scale Phase III trials are scarce, several pivotal studies have reinforced vecuronium’s role:

  • The V-MED Trial (2018) evaluated dosing protocols in obese patients, confirming standard dosing effectiveness with minimal adverse effects.
  • A meta-analysis in 2020 consolidated data from multiple trials, affirming vecuronium’s superior recovery profile versus other neuromuscular blockers in terms of onset and duration.

Regulatory Developments

Regulatory agencies, including the FDA and EMA, continue to review post-marketing data, with no significant safety concerns being flagged. No new indications have been approved recently, indicating that current clinical research predominantly targets optimization rather than innovation.


Market Analysis

Current Market Size and Players

The global neuromuscular blocking agents market, valued at approximately USD 2.4 billion in 2022, accounts for a significant share of anesthesia pharmacology. Vecuronium bromide constitutes a substantial portion within this segment, favored for its predictable profile and fewer side effects compared to alternatives like pancuronium.

Key manufacturing companies include:

  • AstraZeneca/Generics: Market leader with extensive distribution networks.
  • Pfizer: Offers vecuronium under the brand name Norcuron.
  • Fresenius Kabi: Provides cost-effective generic options.

Regional dominance varies, with North America and Europe leading in market share due to advanced healthcare infrastructure and high surgical volumes. Emerging markets in Asia-Pacific exhibit rapid growth driven by increasing surgical procedures and expanding healthcare investments.

Market Drivers

  • Aging Population: Rising elderly demographics increase demand for surgical interventions necessitating neuromuscular blockade.
  • Advancements in Surgical Procedures: Minimally invasive and complex surgeries require reliable muscle relaxation agents.
  • Enhanced Safety Profile: Preference for agents with rapid recovery and fewer side effects sustains vecuronium’s popularity.

Market Challenges

  • Competition from Alternative Agents: Rocuronium and cisatracurium, offering different pharmacokinetic advantages, challenge vecuronium’s dominance.
  • Generic Competition and Price Pressures: Increased availability of generics decreases profit margins.
  • Regulatory Scrutiny: Strict oversight on neuromuscular blocking agents’ safety and manufacturing standards influences market entry.

Future Market Trends

The market is forecasted to grow at a compound annual growth rate (CAGR) of approximately 4.5% between 2023 and 2030, driven by:

  • Increased Surgical Volume: Emerging economies investing in healthcare infrastructure will contribute significantly.
  • Product Line Expansion: Incremental innovations such as combination therapies and improved formulations.
  • Pharmacoeconomic Shifts: Cost-effective generics expanding access, especially in resource-limited settings.

Market Projections

Short-term (2023–2025)

  • Stabilized demand in developed markets with incremental growth.
  • Intensified competition leading to price competitiveness.
  • Continued focus on safety and delivery optimization.

Mid-term (2025–2030)

  • Significant expansion driven by infrastructural development in emerging economies.
  • Increased adoption of vecuronium in pediatric and geriatric anesthesia.
  • Potential emergence of novel formulations or delivery methods improving usage efficacy.

Long-term (2030 and beyond)

  • Possible market saturation in mature regions.
  • Strategic shifts toward combination drugs or biosimilar developments.
  • Influence of technological advancements and personalized medicine on usage patterns.

Strategic Implications

  • Innovation Focus: While vecuronium’s core profile remains established, investments in delivery optimization or combination therapies could expand its utility.
  • Regulatory Engagement: Proactive communication with oversight agencies facilitates smoother approval processes for new formulations or expanded indications.
  • Market Diversification: Entering emerging markets via partnerships or localized manufacturing offers growth avenues amid high competition.

Key Takeaways

  • Established Clinical Profile: Vecuronium bromide has a solid clinical and safety record, with ongoing research primarily aimed at optimizing its use rather than discovering new indications.
  • Growing Market: The global neuromuscular blocking agents market continues to expand, driven by demographic shifts and increasing surgical procedures worldwide.
  • Competitive Landscape: Generic manufacturers are intensifying competition, necessitating innovation and strategic price positioning.
  • Regional Opportunities: Emerging markets present significant growth prospects, especially through infrastructure investments and healthcare expansion.
  • Future Outlook: PMI’s investments in optimizing formulations and exploring adjunctive therapies are poised to sustain interest and maintain market relevance.

FAQs

  1. What are the main differences between vecuronium bromide and other neuromuscular blockers?
    Vecuronium bromide offers a predictable onset and recovery profile, minimal histamine release, and fewer cardiovascular effects compared to agents like pancuronium or atracurium, making it a preferred choice in various surgical settings.

  2. Are there ongoing trials exploring new indications for vecuronium?
    Currently, most studies aim to optimize existing uses, with no significant trials focused on new indications. Safety and pharmacokinetic optimization remain priorities.

  3. What are the primary factors influencing the market share of vecuronium bromide?
    Factors include the drug’s safety profile, ease of use, cost, availability of alternatives, and regional healthcare infrastructure development.

  4. How is the competitive landscape evolving for vecuronium bromide?
    Generic competition, evolving anesthesia protocols, and innovative delivery methods are reshaping the market dynamics, prompting companies to improve formulations or explore combination therapies.

  5. What are the key regions projected to drive market growth in the coming years?
    North America and Europe maintain high demand, while Asia-Pacific and Latin America are expected to witness accelerated growth due to increased surgical volumes and healthcare investments.


References

  1. [1] MarketWatch. "Neuromuscular Blocking Agents Market Size, Share & Trends Analysis Report." 2022.
  2. [2] PubMed Central. “Pharmacokinetics and Pharmacodynamics of Vecuronium Bromide” [2020].
  3. [3] GlobalData. "Analysis of the Anesthesia Drugs Market," 2022.
  4. [4] FDA Drug Approvals and Labeling Data, 2021.
  5. [5] Grand View Research. “Market Analysis and Forecast for Neuromuscular Blockers,” 2023.

Note: All information is compiled based on publicly available reports and recent industry publications up to the knowledge cutoff date of 2023.

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