MP0250 DARPin® Protein Plus Osimertinib in Patients With EGFR-mutated NSCLC
Stopped early · Phase 1
Conditions studied: EGFR-mutated NSCLC (Disorder)
In brief
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.
Key facts
- Study ID
- NCT03418532
- Run by
- Molecular Partners AG
- People needed
- 8
- Starts
- 2018-03-22
- Expected to finish
- 2020-04-24
- Last updated by the study team
- 2023-03-23
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Histologically confirmed metastatic or unresectable locally advanced non-squamous NSCLC with documented EGFR mutation-positive disease
- Radiologically documented disease progression on previous osimertinib treatment.
- Radiologically documented disease progression on or after most recent antitumor therapy.
- Measurable disease according to RECIST 1.1.
- Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0 2.
- Men and women ≥18 years old on the day of signing informed consent.
- Adequate hematological, hepatic and renal function prior to first dose
- Serum albumin concentration ≥30 g/L
- Potassium and magnesium within normal range
You may not qualify if…
- Necrotic tumors or tumors close to large blood vessels that may impose an increased bleeding risk when treated with anti-VEGF agents.
- Second malignancy that is currently clinically significant or required active intervention during the period of 12 months prior to Screening, except early stage non-melanoma skin cancer treated with curative intent.
- Known pre-existing interstitial or inflammatory lung disease.
- Clinical signs of or documented leptomeningeal carcinomatosis. Features such as headache, nuchal rigidity, and photophobia may indicate meningeal involvement.
- Known brain metastases who are clinically unstable
- Prohibited anti-NSCLC therapies and not having recovered from related AEs to Common Terminology Criteria for Adverse Events (CTCAE) Grade ≤1
- Any investigational drug within 28 days prior to study treatment.
- Current participation in any other interventional clinical study (except survival follow up).
- Neuropathy as residual toxicity after prior antitumor therapy Grade >2
- Patients taking medications that have the potential to prolong the QT interval
- Significant cardiac abnormalities
- Uncontrolled hypertension
- Significant risk for bleeding
- Active or recent thrombolic events
Where it is running
- Scottsdale Healthcare Hospitals — Scottsdale, Arizona, United States
- City of Hope - Comprehensive Cancer Center — Duarte, California, United States
- University of California — San Diego, California, United States
- UCLA Medical Center — Santa Monica, California, United States
- Georgetown University — Washington D.C., District of Columbia, United States
- Florida Hospital — Orlando, Florida, United States
- Duke Cancer Institute — Durham, North Carolina, United States
- Tennessee Oncology — Nashville, Tennessee, United States
- UT Southwestern Medical Center — Dallas, Texas, United States
- Oncology Consultants — Houston, Texas, United States
Full record on ClinicalTrials.gov
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