PHASE I RESEARCH
IN CINCINNATI
Contact Dr. Lindsey Wood at (513) 769-2770.New Horizons Clinical Research has been conducting Phase II, III and IV clinical research for over 25 years, and we are pleased to announce we can now offer a complete range of Phase I Services. Our new, state of the art research facility, located in Cincinnati, OH, can accommodate up to 24 subjects, with full amenities for both study volunteers and sponsors.
Research Capabilities (Phase I)
The Phase I unit is designed to conduct studies in healthy volunteers or in patient populations. Types of studies include:
- Pharmacokinetics
- Bioequivalence/Bioavailability
- Safety and Efficacy
- Drug Interaction
- Dose Ranging
- Food effects
Our facility is conveniently located at:
9395 Kenwood Road, Suite 101,
Cincinnati, OH 45242
Local Medical Partners and Resources 9395 Kenwood Road, Suite 101,
Cincinnati, OH 45242
New Horizons Clinical Research Phase I facility is conveniently located in the center of Blue Ash, close to highways and hospitals. We have good working relationships with local hospitals in areas such as clinical laboratory, emergency department, imaging
(X-ray, MRI, CAT scan) and dietary services.
Important Features - Located about one mile from an Emergency Department (Jewish Hospital) and less than one and a half miles from Emergency Responders (Blue Ash Fire Dept.)
- Trained, experienced Phase I research staff, including experience with First-in-Man trials.
- Board-certified principal investigators and sub-investigators.
- Proven record for quality data and surpassing sponsor enrollment goals.
- Security and surveillance 24/7 to ensure study volunteers' safety.
- Ample -70C freezer storage for bioanalytical samples.
- Secured facilities for study medication storage.
- Spacious sleeping quarters and comfortable dining/recreation areas designed for patient comfort.
- Modern examination rooms and lab facilities.
- Computerized database of compliant, healthy volunteers and research patients.
- Consistent history of excellent FDA and sponsor audits.
We have worked with Sponsors ranging from large Pharma to small biotech, and we can offer services from protocol development to proof of concept studies to more typical PK trials; in healthy normals or in defined patient populations. We can work with central or local IRBs to meet the Sponsor’s needs.
For more information about our Phase I Unit, contact Dr. Lindsey Wood at (513) 769-2770
For more information about our Phase I Unit, contact Dr. Lindsey Wood at (513) 769-2770
