Clinical Trials
2
Trial Phases
2 Phases
Drug Approvals
0
Drug Approvals
No drug approvals found
This company may not have drug approvals in our database
Clinical Trials
Distribution across different clinical trial phases (2 trials with phase data)• Click on a phase to view related trials
The Safety and Effectiveness of Retrovir Plus HIVID Combined With Either Nevirapine or Invirase in the Treatment of HIV Infection
- Conditions
- HIV Infections
- First Posted Date
- 2001-08-31
- Last Posted Date
- 2005-06-24
- Lead Sponsor
- Parexel
- Target Recruit Count
- 225
- Registration Number
- NCT00002347
- Locations
- 🇺🇸
PAREXEL Intl Corp / InterCo Collaboration Ctr, Waltham, Massachusetts, United States
News
Harbour BioMed Appoints Yajie Li as Chief Medical Officer to Advance Antibody Therapeutics Pipeline
Harbour BioMed has appointed Yajie Li as Chief Medical Officer to lead clinical development and regulatory strategy for the company's immunology and oncology programs.
Panthera Biopartners Secures £20M in Clinical Trial Contracts Amid UK SMO Sector Growth
Panthera Biopartners, the UK's largest Site Management Organisation, has signed two clinical trial contracts worth over £10 million each with international pharmaceutical companies.
Advarra Integrates eIRB with Study Collaboration Platform to Streamline Clinical Trial Startup
Advarra has integrated its electronic institutional review board (eIRB) system with Study Collaboration software, creating an automated connection between IRB review status and study startup workflows.
Clinical Trial Outsourcing Market Set to Reach $91.2 Billion by 2034, Driven by Technology Integration and Strategic Partnerships
• The global clinical trial outsourcing market is projected to grow from $43.1 billion in 2025 to $91.2 billion by 2034, representing a robust CAGR of 7.46% as pharmaceutical companies increasingly rely on CROs to streamline research processes. • Advanced technologies including AI, machine learning, and blockchain are transforming clinical trial management, enhancing efficiency and accelerating drug approvals while creating new opportunities for market participants. • North America dominates the market due to its strong pharmaceutical industry and favorable regulatory environment, while Asia-Pacific is emerging as a high-growth region offering cost advantages and large patient populations.
Effective Sponsor Oversight Critical for CRO Partnerships in Clinical Trials, Industry Leaders Emphasize
• Clinical trial sponsors and CROs must establish optimal oversight balance, with experts warning that both excessive and insufficient monitoring can impede trial success and efficiency. • Industry leaders at Veeva's Clinical Operations Outsourcing 2024 Forum stress the importance of early collaboration agreements and transparent communication between sponsors and CROs. • As clinical trials become increasingly complex, particularly in specialized therapies, the need for efficient sponsor oversight becomes more crucial for ensuring trial quality and regulatory compliance.
FDA Expedited Designations: RMAT and Fast Track Gain Traction Over Breakthrough Therapy
Parexel's analysis reveals trends in FDA expedited designations for advanced therapies, highlighting Breakthrough Therapy Designation (BTD), Regenerative Medicine Advanced Therapy (RMAT), and Fast Track (FT).
Cultural Adaptation and Flexibility Key to Improving Diversity in Diabetes Clinical Trials
A Feinstein Institutes study demonstrates that culturally tailored telemonitoring interventions significantly improve participation among Hispanic and Latinx communities with type 2 diabetes, reducing HbA1c levels from 8.32% to 7.55%.
NIHR Hosts Expert Panel on Advancing Equality and Diversity in Clinical Research
The National Institute for Health and Care Research (NIHR) is organizing a webinar on January 30, 2024, to address equality, diversity, and inclusion challenges in clinical trial participation.
South Korea Emerges as Premier Clinical Trial Hub with $20 Billion Pharmaceutical Market Potential
South Korea has established itself as a global clinical trial hub, supported by government incentives, modern infrastructure, and streamlined regulatory processes that rank it among the top 15 countries for clinical trials.