Evidence map›Paper›PMID 34309241›Full record

Trial reportPharmacology research & perspectives2021

TROIKA-1: A double-blind, randomized, parallel group, study aimed to demonstrate the equivalent pharmacokinetic profile of HD201, a potential biosimilar candidate to trastuzumab, versus EU-Herceptin

Martin Demarchi, Pierre Coliat, Kristi Mclendon, Jocelyn Chung Shii Hii, Peggy Feyaerts, Felicia Ang, Litha Jaison, Filip Deforce, Marie Paule Derde, Michael Jinwoo Kim and 3 more

Registry-linked trialOpen access · goldAbstract readClinical Trial, Phase IRandomized Controlled TrialEquivalence Trial
In one paragraph

Trial report in Pharmacology research & perspectives, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03776240 (A Phase I, Double-Blind, Randomised, Parallel Group Study to Demonstrate the Equivalent Pharmacokinetic Properties of a Single Intravenous Dose of HD201 and EU-Herceptin® and US-Herceptin® in Healthy Male Subjects), which is not on this map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 46% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03776240 phase1completednot on this map

A Phase I, Double-Blind, Randomised, Parallel Group Study to Demonstrate the Equivalent Pharmacokinetic Properties of a Single Intravenous Dose of HD201 and EU-Herceptin® and US-Herceptin® in Healthy Male Subjects

TypeinterventionalSponsorPrestige Biopharma LimitedRan2019 to 2019Enrolled105ConditionsHealthy VolunteersArmsHD201, EU-Herceptin, US-Herceptin
3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 5 institutions in 5 countries.

Martin DemarchiInstitute of Cancer Strasbourg (ICANS), Strasbourg, France.ORCID 0000-0003-1894-3560
Pierre ColiatInstitute of Cancer Strasbourg (ICANS), Strasbourg, France.
Kristi MclendonRoyal Brisbane and Women's Hospital, Brisbane, Australia.
Jocelyn Chung Shii HiiPrestige Biopharma Ltd, Singapore, Singapore.
Peggy FeyaertsPrestige Biopharma Ltd, Singapore, Singapore.
Felicia AngPrestige Biopharma Ltd, Singapore, Singapore.
Litha JaisonPrestige Biopharma Ltd, Singapore, Singapore.
Filip DeforceDICE, NV, Brusseles, Belgium.
Marie Paule DerdeDICE, NV, Brusseles, Belgium.
Michael Jinwoo KimPrestige Biopharma Ltd, Singapore, Singapore.
Lisa Soyeon ParkPrestige Biopharma Ltd, Singapore, Singapore.
Alexandre DetappePaul Strauss Cancer Center, Strasbourg, France.
Xavier PivotInstitute of Cancer Strasbourg (ICANS), Strasbourg, France.
Institut de Cancérologie Strasbourg · FRSingapore Clinical Research Institute · SGRode Kruis-Vlaanderen · BEUS Biologic (United States) · USRoyal Brisbane and Women's Hospital · AU

Funding

Prestige Biopharma Ltd
6 · The paper itself

Abstract

Prestige Biopharma Ltd (Singapore) has developed HD201, a proposed biosimilar to reference product trastuzumab. As a part of the stepwise approach to ensure comparability between the biosimilar candidate and the reference medicinal product, a phase I study in healthy subjects was conducted to demonstrate the pharmacokinetic (PK) equivalence (NCT03776240). The primary objective of the study was to demonstrate (PK) equivalence of HD201, EU-Herceptin

Indexed as

AdolescentAdultAntibodiesAntineoplastic Agents, ImmunologicalArea Under CurveBiosimilar PharmaceuticalsDouble-Blind MethodHealthy VolunteersHumansInfusions, IntravenousMaleMiddle AgedTrastuzumabYoung AdultAntibodiesAntineoplastic Agents, ImmunologicalBiosimilar PharmaceuticalsTrastuzumabbiosimilarpharmacokinetictrastuzumab

Identifiers

PMID34309241
PMCPMC8311913
OpenAlexW3184426087

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.