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A phase I, randomized, double-blind, placebo-controlled, four-way cross-over study to evaluate the analgesic effects of TRV045 in healthy adults

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2022-501804-80-00
Acronym
CP045-1002
Enrollment
24
Registered
2022-11-15
Start date
2022-11-17
Completion date
2023-06-21
Last updated
2023-03-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute and chronic neuropathic pain secondary to diabetic peripheral neuropathy

Brief summary

Pharmacodynamic measurements with the UVB pain model

Detailed description

Pharmacokinetic endpoints, Safety and tolerability endpoints

Interventions

Sponsors

Trevena Inc.
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to 64 Years

Design outcomes

Primary

MeasureTime frame
Pharmacodynamic measurements with the UVB pain model

Secondary

MeasureTime frame
Pharmacokinetic endpoints, Safety and tolerability endpoints

Countries

Netherlands

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026