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2025-523410-84-00Not yet recruitingPhase 1

An open label, balanced, randomized, two-treatment, two-period, two-sequence, single dose crossover, bioavailability study comparing Bupropion Hydrochloride Extended Release Capsules 150 mg, Manufactured by Sun Pharmaceutical Industries Limited, India with WELLBUTRIN XL (Bupropion hydrochloride) extended release tablets 300 mg, Distributed by: Bausch Health US, LLC Bridgewater, NJ 08807 USA. Manufactured by: Bausch Health Companies, Inc. Steinbach, MB R5G 1Z7, Canada, in healthy, adult, human subjects under fasting condition.

Source: EU CTIS (euclinicaltrials.eu) · Last updated 5 May 2026

Next steps

Status (registry)
Not yet recruiting
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
72 (estimated)
First submitted
28 Jan 2026
Start date
1 Jun 2026
Lead sponsor
Sun Pharmaceutical Industries Limited
EU CT number
2025-523410-84-00

What you commit to

  • Study type: Interventional · Phase 1
  • Planned participants: 72
  • 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.

AI-kivonat: who the study is looking for

Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for healthy adults to compare two forms of bupropion hydrochloride extended release (150 mg capsules and 300 mg tablets) taken as a single dose while fasting.

Age
18 to 64 years
Sex
Women and men can join.

Read by machine on 9 Nov 2026.

Sites (1)

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

SiteCityCountrySite status
Terapia S.A.Cluj-NapocaRomaniaNot yet recruiting

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