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2023-507991-32-00CompletedPhase 1

An open label, balanced, randomized, single dose, two treatment, two period, two sequence, crossover, bioequivalence study comparing Lacosamide tablets USP 200 mg, manufactured by Sun Laboratories Industries Limited, India with Vimpat (Lacosamide) 200 mg film-coated tablets, Marketing Authorisation Holder UCB Pharma S.A., Belgium, in healthy adult, human subjects under fasting condition.

Source: EU CTIS (euclinicaltrials.eu) · Last updated 19 Feb 2024

Next steps

Status (registry)
Completed
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
32 (actual)
First submitted
26 Oct 2023
Start date
25 Jul 2024
Lead sponsor
Sun Pharmaceutical Industries Limited
EU CT number
2023-507991-32-00

What you commit to

  • Study type: Interventional · Phase 1
  • Participants enrolled: 32
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study design.

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Terapia S.A.Cluj-NapocaRomaniaCompleted

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This page is information, not medical advice. Discuss any trial with your doctor.