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NCT03476993

Non-comparative Study of BCD-085 in Combination With UDCA in Patients With Primary Biliary Cholangitis

Terminated Phase 2 Last updated 11 October 2019
What this trial tests

Phase 2 trial testing BCD-085 in Liver Cirrhosis, Biliary in 9 participants. Terminated before completion.

Timeline
27 April 2018
Primary endpoint
1 July 2019
1 July 2019

Quick facts

Lead sponsorBiocad
PhasePhase 2
StatusTerminated
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment9
Start date27 April 2018
Primary completion1 July 2019
Estimated completion1 July 2019
Sites3 locations across Russia

Drugs / interventions tested

Conditions studied

Sponsor

Biocad — full company profile →

Who can join

Adults 18 to 60, any sex, with Liver Cirrhosis, Biliary. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

BCD-085 is an innovative drug, anti-interleukin-17 monoclonal antibody. The aim of the study is to evaluate the efficacy and safety of BCD-085 in patients with primary biliary cholangitis (PBC).

Publications & conference data

2 peer-reviewed publications reference this trial (live from Europe PMC):

  1. Targeting interleukin-17 in chronic inflammatory disease: A clinical perspective.
    Zwicky P, Unger S, Becher B. · · 2020 · cited 66× · PMID 31727781 · DOI 10.1084/jem.20191123
  2. Novel Therapies for Managing Cholestasis.
    Santiago P, Levy C. · · 2020 · cited 3× · PMID 32257119 · DOI 10.1002/cld.886

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Other trials of BCD-085

Trials testing the same drug.

Other Biocad trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03476993.

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