Abstract connected dots and lines

Discuss your clinical development program.

Obesity trials require reliable recruitment, participant retention, protocol discipline and coordinated execution across clinical, operational and data teams. DVCR helps sponsors execute these studies with early phase experience in overweight and obese populations, a purpose-built Phase I unit and integrated services from startup through reporting.

Obesity study experience

DVCR’s clinic, recruitment, study management and clinical operations teams have supported more than 10 overweight and obese volunteer trials in the past decade.

Project management depth

DVCR’s project management team has conducted more than 25 trials in overweight and obese populations, supporting coordinated execution from startup through closeout.

Purpose-built Phase I unit

A 100-bed Phase I unit supports overnight trials, participant comfort, retention and controlled early phase study conduct.

Early phase CRO support

DVCR supports FIH, SAD/MAD, clinical pharmacology, Phase Ib/IIa proof-of-concept and Phase I-II multi-site patient trials.

Integrated study execution

Project management, data management, biostatistics, statistical programming, PK/PD analysis and modeling, clinical and medical monitoring, medical writing as well as site feasibility, management and central laboratory services for Phase I-II multi-site trials with our global network of site partners.

Technology-enabled data quality

Integrated systems support real-time data capture, sponsor visibility, audit-ready documentation and cleaner study conduct.

Science, teamwork and scientist with tablet in laboratory

DVCR’s regional footprint and volunteer database support recruitment for overweight and obese participant populations, including individuals across BMI ranges commonly required in cardiometabolic and obesity protocols.

Key database counts:

  • BMI 27.0–35.0 kg/m²: 8,077 volunteers
  • BMI 30.0–40.0 kg/m²: 5,297 volunteers
  • BMI 30.0–45.0 kg/m²: 5,866 volunteers