Clinical Trials Directory

Trials / Completed

CompletedNCT04430842

Dose Escalation Study to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of QBS10072S

A Phase 1, Open Label, Multi-Center, Single and Multiple Dose, Dose Escalation and Expansion Study to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of QBS10072S in Previously Treated Patients With Advanced or Metastatic Cancers With High LAT1 Signatures, and in Patients With Relapsed or Refractory Grade 4 Astrocytoma

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
15 (actual)
Sponsor
Quadriga Biosciences, Inc. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This is a multi-center, open-label, dose escalation study to determine the safety, tolerability, pharmacokinetics, pharmacodynamics, and maximum tolerated dose (MTD) of QBS10072S in patients with advanced or metastatic cancers with high LAT1 expression. The MTD of QBS10072S will be confirmed in patients with relapsed or refractory grade 4 astrocytoma.

Conditions

Interventions

TypeNameDescription
DRUGQBS10072SQBS10072S targets cancers with high LAT1 expression.

Timeline

Start date
2020-07-20
Primary completion
2022-09-21
Completion
2022-12-22
First posted
2020-06-12
Last updated
2023-01-18

Locations

2 sites across 1 country: Australia

Source: ClinicalTrials.gov record NCT04430842. Inclusion in this directory is not an endorsement.