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2023-506163-34-00CompletedPhase 3

Efficacy and safety of the proposed biosimilar PERT-IJS versus EU-Perjeta® along with trastuzumab and chemotherapy (carboplatin and docetaxel) as neoadjuvant treatment in chemotherapy naïve patients with early stage or locally advanced HR negative and HER2 positive breast cancer

Source: EU CTIS (euclinicaltrials.eu) · Last updated 27 Nov 2023

Next steps

Status (registry)
Completed
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
46 (actual)
First submitted
28 Jul 2023
Start date
24 Nov 2023
Lead sponsor
Biocon Biologics UK Limited
EU CT number
2023-506163-34-00

What you commit to

  • Study type: Interventional · Phase 3
  • Participants enrolled: 46
  • 10 sites in 2 countries
  • 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 (10)

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

SiteCityCountrySite status
Wojewodzki Szpital Specjalistyczny W Bialej PodlaskiejBiala PodlaskaPolandCompleted
Szpital Specjalistyczny Im. Ludwika Rydygiera W Krakowie Sp. z o.o.CracowPolandCompleted
Pratia S.A.CracowPolandCompleted
Instytut MSF Sp. z o.o.LodzPolandCompleted
Centra Medyczne Medyceusz Sp. z o.o.LodzPolandCompleted
Mruk-Med I Sp. z o.o.RzeszówPolandCompleted
Narodowy Instytut Onkologii im Marii Sklodowskiej Curie Panstwowy Instytut BadawczyWarsawPolandCompleted
Spital Clinic Militar De Urgenta Dr. Constantin Papilian Cluj NapocaCluj-NapocaRomaniaCompleted
Centrul De Oncologie SF Nectarie S.R.L.CraiovaRomaniaCompleted
Sigmedical Services S.R.L.SuceavaRomaniaCompleted

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