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Terminated Phase 1 Interventional

MP0250 DARPin® Protein Plus Osimertinib in Patients With EGFR-mutated NSCLC

ClinicalTrials.gov ID: NCT03418532

Public ClinicalTrials.gov record NCT03418532. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 10:18 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 1b/2, Single-arm, Open-label, Multi-center Study of MP0250 in Combination With Osimertinib in Patients With EGFR-mutated Non-squamous Non-small Cell Lung Cancer (NSCLC) Pretreated With Osimertinib

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to assess the anti-tumor efficacy, safety, tolerability, pharmacokinetics (PK), immunogenicity and biological activity of the MP0250 DARPin® drug candidate in combination with osimertinib orally once daily (o.d.), when administered to patients with EGFR mutated, advanced, non squamous NSCLC after tumor progression on osimertinib and on or after the most recent therapy. MP0250 is a multi-DARPin® protein with three specificities, able to simultaneously neutralize the activities of vascular endothelial growth factor (VEGF) and hepatocyte growth factor (HGF) and also to bind to human serum albumin (HSA) to give an increased plasma half-life and potentially enhanced tumor penetration.

Study identification

NCT ID
NCT03418532
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1
Lead sponsor
Molecular Partners AG
Industry
Enrollment
8 participants

Conditions and interventions

Interventions

Combination Product

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 22, 2018 (Actual)
Primary completion
Aug 30, 2019 (Actual)
Completion
Apr 24, 2020 (Actual)
Last update posted
Mar 23, 2023

2018 – 2020

United States locations

U.S. sites
10
U.S. states
7
U.S. cities
10
Facility City State ZIP Site status
Scottsdale Healthcare Hospitals Scottsdale Arizona 85258 —
City of Hope - Comprehensive Cancer Center Duarte California 91010 —
University of California San Diego California 92093 —
UCLA Medical Center Santa Monica California 90404 —
Georgetown University Washington D.C. District of Columbia 20057 —
Florida Hospital Orlando Florida 32803 —
Duke Cancer Institute Durham North Carolina 27710 —
Tennessee Oncology Nashville Tennessee 37203 —
UT Southwestern Medical Center Dallas Texas 75390 —
Oncology Consultants Houston Texas 77030 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03418532, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 23, 2023 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03418532 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →