Lung Cancer Clinical Trial

Patritumab Deruxtecan in Combination With Osimertinib in Subjects With Locally Advanced or Metastatic EGFR-mutated Non-Small Cell Lung Cancer

Summary

This study includes a Dose Escalation Part to identify the recommended combination dose (RCD) and a Dose Expansion Part to further evaluate efficacy and safety.

The primary objectives:

Dose Escalation: To assess the safety and tolerability of patritumab deruxtecan (U3-1402) and osimertinib in subjects with locally advanced or metastatic non-small cell lung cancer (NSCLC) with an EGFR exon 19 deletion or L858R mutation with tumor progression after treatment with osimertinib, and to determine the recommended combination dose (RCD).

Second-Line Dose Expansion Arm 1 and Arm 1b: To assess the preliminary antitumor activity of patritumab deruxtecan and osimertinib in subjects with locally advanced or metastatic NSCLC with an EGFR exon 19 deletion or L858R mutation with tumor progression after treatment with osimertinib. Note: One or both of the study arms may open with one or two distinct dosing schedules.

Second-Line Dose Expansion Arm 2: To assess the preliminary antitumor activity of patritumab deruxtecan monotherapy in subjects with locally advanced or metastatic NSCLC with an EGFR exon 19 deletion or L858R mutation with tumor progression after treatment with osimertinib.

First-Line Dose Expansion: To assess the safety and tolerability of patritumab deruxtecan and osimertinib in subjects with locally advanced or metastatic NSCLC with an EGFR exon 19 deletion or L858R mutation without prior systemic treatment for locally advanced or metastatic disease.

View Full Description

Full Description

Dose Escalation:

Population includes subjects with locally advanced or metastatic NSCLC with an EGFR exon 19 deletion or L858R mutation with tumor progression after treatment with osimertinib. The starting combination dose regimen is patritumab deruxtecan 3.2 mg/kg IV every 21 days (Q3W) and osimertinib 80 mg orally (PO) once daily. At least 3 to 6 subjects will be enrolled in each cohort.

Dose Expansion: Two subject populations will be evaluated in the Dose Expansion Part:

Second-Line: Subjects with locally advanced or metastatic NSCLC with an EGFR exon 19 deletion or L858R mutation with tumor progression after treatment with osimertinib
First-Line: Subjects with locally advanced or metastatic NSCLC with an EGFR exon 19 deletion or L858R mutation, and without prior systemic therapy for advanced or metastatic disease. Note: The first line expansion will only be initiated if the RCD includes osimertinib 80 mg PO once daily.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Inclusion Criteria Specific to Dose Escalation and Second-Line Dose Expansion:

Documentation of EGFR exon 19 deletion or L858R mutation detected from tumor tissue
Must have received osimertinib for locally advanced or metastatic disease at a dose of 80 mg once daily (QD) for at least 6 weeks and must not miss more than two doses during the 2 weeks prior to the first day of study treatment (Cycle 1, Day 1)
Must not have received any other prior systemic cancer therapies in the locally advanced/metastatic setting
Has documentation of radiological disease progression following first-line treatment with osimertinib in the locally advanced or metastatic setting

Inclusion Criteria Specific to First-line Dose Expansion:

The tumor tissue harbors one of the 2 common EGFR mutations occurring in NSCLC known to be associated with EGFR-TKI sensitivity (exon 19 deletion or L858R) as assessed by Clinical Laboratory Improvement Amendments (CLIA)-certified (United States [US] sites), accredited (outside of the US), local laboratory or central laboratory. Only tissue-based testing will be accepted.
Participants must have previously untreated locally advanced or metastatic NSCLC and must be eligible to receive first-line treatment with osimertinib, according to the judgment of the investigator. Prior adjuvant or neo-adjuvant therapy (chemotherapy, radiotherapy, investigational agents; except with osimertinib) is permitted.

All Participants:

Participants must meet all criteria to be eligible for inclusion in this study:

Histologically or cytologically documented locally advanced or metastatic NSCLC not amenable to curative surgery or radiation.
At least 1 measurable lesion as assessed by Investigator as per Response Evaluation Criteria in Solid Tumors (RECIST v1.1)

For Second-Line Dose Expansion (Arm 1, Arm 2, and Arm 1b) and First-Line Dose Expansion (Cohort 3), willing to provide required tumor tissue of sufficient quantity (as defined in the laboratory manual) with adequate tumor tissue content (as confirmed by hematoxylin and eosin staining at central laboratory). The pre-treatment biopsy is optional for participants enrolled in the Dose Escalation Part (all cohorts). Required tumor tissue can be provided as either:

Pre-treatment tumor biopsy from at least 1 lesion not previously irradiated and amenable to core biopsy OR
Archival tissue collected from a biopsy performed within 3 months prior to signing of the tissue consent and since progression while on the most recent cancer therapy regimen.
On-study tumor biopsy is optional in Dose Escalation.

Has adequate bone marrow reserve and organ function based on local laboratory data within 14 days prior to Cycle 1, Day 1 (Dose Escalation and First-Line Dose Expansion) or within 14 days prior to randomization (Second-Line Dose Expansion):

Platelet count: ≥100 000/mm^3 or ≥100 × 10^9/L (platelet transfusions are not allowed up to 14 days prior to Cycle 1, Day 1 to meet eligibility)
Hemoglobin: ≥9.0 g/dL (transfusion and/or growth factor support is allowed)
Absolute neutrophil count ; 1500/mm^3 or ≥1.5 × 10^9/L
Serum creatinine (SCr) OR creatinine clearance (CrCl): SCr ≤1.5 × ULN, OR CrCl ≥30 mL/min as calculated using the Cockcroft-Gault equation or measured CrCl; confirmation of CrCl is only required when creatinine is >1.5 × ULN
Aspartate aminotransferase/ alanine aminotransferase: ≤3 × ULN (if liver metastases are present, ≤5 × ULN)
Total bilirubin: ≤1.5 × ULN if no liver metastases (<3 × ULN in the presence of documented Gilbert's syndrome [unconjugated hyperbilirubinemia] or liver metastases)
Serum albumin ; ≥2.5 g/dL
Prothrombin time (PT) or PT-international normalized ratio (INR) and Activated partial thromboplastin time (aPTT) / Partial thromboplastin time (PTT): ≤1.5 × ULN, except for subjects on coumarin-derivative anticoagulants or other similar anticoagulant therapy, who must have PT-INR within therapeutic range as deemed appropriate by the Investigator.

Exclusion Criteria:

Any previous histologic or cytologic evidence of small cell OR combined small cell/non-small cell disease in the archival tumor tissue or pre-treatment tumor biopsy.
Any history of interstitial lung disease (including pulmonary fibrosis or radiation pneumonitis), has current interstitial lung disease (ILD), or is suspected to have such disease by imaging during screening.

Clinically severe pulmonary compromise (based on Investigator's assessment) resulting from intercurrent pulmonary illnesses including, but not limited to:

Any underlying pulmonary disorder (eg, pulmonary emboli within three months of the study enrollment or randomization, severe asthma, severe chronic obstructive pulmonary disease, restrictive lung disease, pleural effusion);
Any autoimmune, connective tissue or inflammatory disorders with pulmonary involvement (eg, rheumatoid arthritis, Sjogren's syndrome, sarcoidosis); OR prior complete pneumonectomy.
Is receiving chronic systemic corticosteroids dosed at >10 mg prednisone or equivalent anti-inflammatory activity or any form of immunosuppressive therapy prior to Cycle 1, Day 1 (Dose Escalation and First-Line Dose Expansion) or prior to randomization (Second-Line Dose Expansion). Participants who require use of bronchodilators, inhaled or topical steroids, or local steroid injections may be included in the study.
Evidence of any leptomeningeal disease.
Evidence of clinically active spinal cord compression or brain metastases, defined as untreated and symptomatic, or requiring therapy with corticosteroids or anticonvulsants to control associated symptoms. Participants with clinically inactive or treated brain metastases who are asymptomatic (ie, without neurologic signs or symptoms and do not require treatment with corticosteroids or anticonvulsants) may be included in the study.

Inadequate washout period prior to Cycle 1, Day 1 (Dose Escalation and First-Line Dose Expansion) or prior to randomization (Second-Line Dose Expansion) defined as:

Whole brain radiation therapy <14 days or stereotactic brain radiation therapy <7 days;
Any systemic anticancer (excluding osimertinib in all Dose Escalation Cohorts and in Second-Line Dose Expansion [Arm 1, Arm 2, and Arm 1b]), including investigational agents, <14 days or 5 half-lives, whichever is longer
Immune checkpoint inhibitor therapy <5 half-lives
Major surgery (excluding placement of vascular access) <4 weeks
Radiotherapy treatment to more than 30% of the bone marrow or with a wide field of radiation < 28 days or palliative radiation therapy <14 days
Chloroquine or hydroxychloroquine ≤14 days
Medications or herbal supplemented known to be strong inducers of cytochrome P450 (CYP) 3A4 <21 days.
Has unresolved toxicities from previous anticancer therapy, defined as toxicities (other than alopecia) not yet resolved to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE) version 5.0, Grade ≤1 or baseline. Subjects with chronic Grade 2 toxicities may be eligible per the discretion of the Investigator after consultation with the Sponsor Medical Monitor or designee.
Refractory nausea and vomiting, chronic gastrointestinal diseases, inability to swallow osimertinib, or previous significant bowel resection that would preclude adequate absorption of osimertinib.
Has any primary malignancy other than locally advanced or metastatic NSCLC within 3 years prior to Cycle 1, Day 1 (Dose Escalation and First-Line Dose Expansion) or within 3 years prior to randomization (Second-Line Dose Expansion), except adequately resected non-melanoma skin cancer, curatively treated in situ disease, or other solid tumors curatively treated.

Uncontrolled or significant cardiovascular disease prior to Cycle 1, Day 1 (Dose Escalation and First-Line Dose Expansion) or prior to randomization (Second-Line Dose Expansion) including:

Mean corrected QT interval using Fridericia's formula (QTcF) prolongation interval of >470 ms for females and >450 ms for males in 3 successive screening measurements
Left ventricular ejection fraction (LVEF) <50% by either echocardiogram (ECHO) or multigated acquisition (MUGA) scan
Resting systolic blood pressure >180 mmHg or diastolic blood pressure >110 mmHg
Myocardial infarction within 6 months
New York Heart Association (NYHA) Classes 2 to 4 congestive heart failure within 28 days
Uncontrolled angina pectoris within 6 months
Has cardiac arrhythmia requiring antiarrhythmic treatment
Complete left or right bundle branch block within 6 months
History of second- or third-degree heart block or PR interval >250 ms within 6 months
History of clinically relevant ventricular arrhythmias, such as ventricular tachycardia, ventricular fibrillation, or Torsade de Pointes
Has any factors that increase the risk of corrected QT (QTc) prolongation or risk of arrhythmic events, such as heart failure, hypokalemia, congenital long QT syndrome, family history of long QT syndrome, or unexplained sudden death under 40 years of age in first-degree relatives, or any concomitant medication known to prolong the QT interval
Has clinically significant corneal disease
Any evidence of severe or uncontrolled diseases including active bleeding diatheses, active infection, psychiatric illness/social situations, geographical factors, substance abuse, or other factors which in the Investigator's opinion makes it undesirable for the subject to participate in the study or which would jeopardize compliance with the protocol. Screening for chronic conditions is not required.

Study is for people with:

Lung Cancer

Phase:

Phase 1

Estimated Enrollment:

252

Study ID:

NCT04676477

Recruitment Status:

Recruiting

Sponsor:

Daiichi Sankyo, Inc.

Check Your Eligibility

Let’s see if you might be eligible for this study.

What is your age and gender ?

Submit

There are 11 Locations for this study

See Locations Near You

Massachusetts General Hospital Cancer Center
Boston Massachusetts, 02114, United States More Info
Principal Investigator
Contact
Dana-Farber Cancer Institute
Boston Massachusetts, 02215, United States More Info
Principal Investigator
Contact
Memorial Sloan Kettering Cancer Center
New York New York, 10065, United States More Info
Principal Investigator
Contact
Sarah Cannon and HCA Research Institute
Nashville Tennessee, 37203, United States More Info
Principal Investigator
Contact
Virginia Cancer Specialists, PC
Fairfax Virginia, 22031, United States More Info
Principal Investigator
Contact
National Cancer Center Hospital
Chuo Ku Tokyo, 104-0, Japan More Info
See Central Contact
Contact
National Hospital Organization Kyushu Cancer Center
Fukuoka , 811-1, Japan More Info
See Central Contact
Contact
Shizuoka Cancer Center
Shizuoka , 411-8, Japan More Info
See Central Contact
Contact
The Cancer Institute Hospital of JFCR
Tokyo , 135-8, Japan More Info
Principal Investigator
Contact
Kanagawa Cancer Center
Yokohama , 241-8, Japan More Info
See Central Contact
Contact
Kindai University Hospital
Ōsaka-sayama , 589-8, Japan More Info
See Central Contact
Contact

How clear is this clinincal trial information?

Study is for people with:

Lung Cancer

Phase:

Phase 1

Estimated Enrollment:

252

Study ID:

NCT04676477

Recruitment Status:

Recruiting

Sponsor:


Daiichi Sankyo, Inc.

How clear is this clinincal trial information?

×

Introducing, the Journey Bar

Use this bar to access information about the steps in your cancer journey.