Safety of Effivia®, a Bevacizumab Biosimilar

NCT06313268 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 83

Last updated 2024-10-10

No results posted yet for this study

Summary

This is a post-marketing observational study aimed to evaluated the safety profile of Effivia®, a biosimilar of bevacizumab, in mexican patients with different types of cancer.

Conditions

Interventions

DRUG

Bevacizumab Biosimilar MB02

5 mg/kg to 15 mg/kg in combination with chemotherapy.

Sponsors & Collaborators

  • Servicios Especializados en Ensayos Clínicos, S.C.

    collaborator UNKNOWN
  • Laboratorios Liomont

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-08-11
Primary Completion
2024-04-17
Completion
2024-09-02
FDA Drug
Yes

Countries

  • Mexico

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06313268 on ClinicalTrials.gov