Breast Cancer Clinical Trial

A Study to Evaluate the Safety, Tolerability, and Efficacy of MORAb-202 (Herein Referred to as Farletuzumab Ecteribulin), a Folate Receptor Alpha (FRα)-Targeting Antibody-drug Conjugate (ADC) in Participants With Selected Tumor Types

Summary

The primary objectives of the study are: (1) in the dose-escalation part: to evaluate safety and tolerability and to determine the recommended Phase 2 dose (RP2D) of farletuzumab ecteribulin in participants with selected tumor types (ovarian cancer [OC], endometrial cancer [EC], non-small cell lung carcinoma [NSCLC], triple-negative breast cancer [TNBC]), and (2) in dose-confirmation part: to evaluate preliminary efficacy measured by objective response rate (ORR) of farletuzumab ecteribulin in participants with OC and EC at selected doses and to further evaluate the safety and tolerability of farletuzumab ecteribulin.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Aged >=18 years

For Dose-Escalation: Females (TNBC, EC and OC) or males/females (NSCLC, adenocarcinoma). Participants with the following disease characteristics:

Participants with the following tumor types, each as a separate arm:

TNBC: Histologically confirmed diagnosis of metastatic TNBC (that is, estrogen receptor (ER) negative/progesterone receptor negative/ human epidermal growth factor receptor 2 (HER2) negative (defined as immunohistochemistry (IHC) less than (<) 2 plus (+) or fluorescence in situ hybridization (FISH) negative) breast cancer). Previously treated with at least one line of systemic anticancer therapy (cytotoxic or targeted anticancer agents) in the metastatic setting.
NSCLC adenocarcinoma: Histologically or cytologically confirmed metastatic NSCLC adenocarcinoma: participants who have failed previous treatment for metastatic disease, are not indicated or failed epidermal growth factor receptor (EGFR)-, Anaplastic lymphoma kinase (ALK) -, B-Raf proto-oncogene (BRAF) - or c-ros oncogene 1 (ROS1) - targeted therapy, and for whom no alternative standard therapy exists.
EC: Histologically confirmed diagnosis of advanced, recurrent or metastatic EC. Relapsed or failure of at least one platinum-based regimen or one immunotherapy-based regimen.
OC or primary peritoneal cancer or fallopian tube cancer: Histologically confirmed diagnosis of high grade serous epithelial ovarian cancer or primary peritoneal cancer or fallopian tube cancer.

Participants must have:

platinum-resistant disease (defined as progression within 6 months after the last dose of at least 4 cycles of the last platinum containing chemotherapy regimen)
received up to 4 lines of systemic therapy post development of platinum resistance.

For Dose-Confirmation:

Ovarian cancer or primary peritoneal cancer or fallopian tube cancer:

Platinum-resistant disease:

For participant with 1 line of platinum-containing therapy: RECIST version 1.1 progression greater than (>) 1 month and less than or equal to (<=) 6 months after the last dose of the first platinum-containing chemotherapy regimen (of at least 4 cycles)
For participant with 2-3 lines of platinum-containing therapy: RECIST version 1.1 progression during or within 6 months after the last dose of the 2nd or 3rd platinum-containing chemotherapy regimen.

Have received up to 3 prior lines of systemic therapy and for whom single-agent therapy is appropriate as the next line of therapy. Participants may have been treated with up to one line of therapy subsequent to determination of platinum-resistance.

Neoadjuvant plus/minus (±) adjuvant will be considered 1 line of therapy.
Maintenance therapy (example, bevacizumab, PARP inhibitors) will be considered part of the preceding line of therapy (will not be counted as an independent line of therapy).
Hormonal therapy will be counted as a separate line of therapy unless it was given as maintenance.
Therapy changed due to toxicity in the absence of progression will be considered part of the same line.
Participants must have histologically confirmed diagnosis of advanced, recurrent, or metastatic EC. All histologic (including carcinosarcoma [no more than one participant at any dose level]) and molecular subtypes will be included. Participants may have been treated with an Immune Checkpoint Inhibitor (ICI) containing regimen (or be ineligible for ICI treatment) and must have had no more than 2 prior regimens (not including adjuvant therapy if progression or recurrent/metastatic disease occurred more than 6 months after the completion of the last cycle of adjuvant therapy).
Note: There is no restriction regarding prior hormonal therapy.
Available tumor tissue for FRα expression percent (%) by IHC analysis as assessed by the vendor. There is no minimum requirement for FRα expression (%). However, the tumor sample must be evaluable for IHC analysis (that is, of sufficient quality and quantity). Sample re-submission will be permitted for participants with tissue result of "non-evaluable" who are otherwise eligible. Tumor sample submission must be archival formalin-fixed, paraffin-embedded (FFPE) tissue block , or unstained slides sectioned within 45 days from the latest FFPE block, or a fresh biopsy sample obtained during screening but prior to initiation of study treatment.
Radiological disease progression on or after the most recent therapy by investigator assessment.

Measurable disease meeting the following criteria (confirmed by central radiographic review, in the Dose-Confirmation Part only):

At least one lesion of >1.0 centimeter (cm) in long axis diameter for non-lymph nodes or >1.5 cm in short axis diameter for lymph nodes that is serially measurable according to Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 using either computed tomography (CT) or magnetic resonance imaging (MRI),
Lesions that have had external beam radiotherapy (EBRT) or loco-regional therapies such as radiofrequency (RF) ablation must show evidence of PD based on RECIST 1.1 to be deemed a target lesion.
ECOG PS of 0 or 1.
Participants who are expected to survive a minimum of 3 months after the first administration of the study drug.
Adequate renal function as evidenced by serum creatinine less than or equal to (<=) 1.5 milligram per deciliter (mg/dL) or calculated creatinine clearance >=50 milliliter per (mL) /minute according to a 12 or 24 hour urine collection.

Adequate bone marrow function, as evidenced by:

Absolute neutrophil count (ANC) >=1.0*10^9 per liter (/L)
Hemoglobin (Hgb) >=9.0 gram per deciliter (g/dL)
Platelet count >=75*10^9/L Growth factors or transfusions as per institutional practice, are allowed if needed to achieve the above values. Growth factor and platelet transfusion should not be used within 7 days of initiation of study treatment.

Adequate liver function, as evidenced by:

Total bilirubin <=1.5*upper limit of normal (ULN) except for unconjugated hyperbilirubinemia (example, Gilbert's syndrome)
Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) <=3*ULN (in the case of liver metastases <=5*ULN) unless there are bone metastases. Participants with Alkaline Phosphatase (ALP) <=3*ULN unless they and are known to have bone metastases in which case higher ALP values will also be allowed.
Albumin >3.0 g/dL.

Participants must undergo a washout period required from the end of prior treatment to the first administration of the study drug that will be as follows:

Prior anticancer therapy:

Prior chemotherapy, surgical therapy, radiation therapy: >3 weeks. Prior chest radiotherapy or pneumonectomy is an exclusion.
Antibody and other biologic therapeutic agents: >=4 weeks.
Endocrine therapy or, small-molecule targeted therapy: >2 weeks.
Immunotherapy >=4 weeks.
Participants with a history of deep vein thrombosis (DVT) within 3 months prior must have completed at least 1 month of anticoagulation prior to starting study treatment. Anticoagulation must continue while on study treatment.
Participants at risk for DVT secondary to central venous catheters or with past medical history of DVT or clinical symptoms suggestive of DVT must have venous Doppler ultrasonography to rule out DVT during the screening period and prior to initiation of study treatment.
If a participant has undergone major surgery, the participant must have recovered adequately from the toxicity and/or complications from the intervention prior to starting study treatment.
Resolution of anticancer therapy-related or radiation-related toxicities to Grade 1 severity or lower, except for stable sensory neuropathy (Grade <=2), anemia ([haemoglobin] Hgb >=9.0 g/dL), and alopecia (any grade).
Participant must be willing and able to comply with all aspects of the protocol.
Participant must provide written informed consent prior to any study-specific screening procedures.

Exclusion Criteria:

Participants with endometrial leiomyosarcoma, endometrial stromal sarcoma or high-grade sarcoma.
Participants who received previous treatment with any folate receptor targeting agents.
Participants with platinum refractory ovarian cancer (defined as disease progression during the initial platinum-based chemotherapy treatment).
Currently enrolled in another clinical study or used any investigational drug or device, which in the opinion of the Sponsor may interfere with the study treatment, within the past 28 days or 5 times the half-life (where prior drug therapy falls under the parameters these Inclusion Criteria should be followed) of any investigational drug preceding informed consent.
Participants with brain or subdural metastases are not eligible, unless they have completed local therapy and have discontinued the use of corticosteroids for this indication for at least 2 weeks before starting treatment in this study. Any signs (example, radiologic) or symptoms of brain metastases must be stable for at least 4 weeks before starting study treatment.
Diagnosed with meningeal carcinomatosis.
Any other invasive malignancy that required treatment (other than definitive surgery) or has shown evidence of recurrence/progression (except for non-melanoma skin cancer, or histologically confirmed complete excision of carcinoma in situ) during the 2 years prior to starting study treatment.
Significant cardiovascular impairment. History within 6 months prior to the first dose of study drug of: congestive heart failure greater than New York Heart Association (NYHA) Class II); unstable angina; myocardial infarction; stroke; cardiac arrhythmia associated with hemodynamic instability.
Clinically significant ECG abnormality, including marked prolonged baseline QT as corrected using Fridericia's formula (QTcF) (repeated demonstration of a QTcF interval >500 milliseconds [ms]). A history of risk factors for torsade de pointes (example, heart failure, hypokalemia, family history of long QT Syndrome) or the use of concomitant medications that prolong the QTcF.
Known to be Human Immunodeficiency Virus (HIV) positive. Testing at entry not required.
Active viral hepatitis (B or C as demonstrated by positive serology). Testing at entry if there are no symptoms or history is not required unless as per local requirements.
Females who are breastfeeding or pregnant at Screening or Baseline (as documented by a positive beta human chorionic gonadotropin [ß-hCG] or human chorionic gonadotropin [hCG]) with a minimum sensitivity of 25 International units per liter (IU/L) or equivalent units of ß-hCG [or hCG]. A separate baseline assessment is required if a negative screening pregnancy test was obtained more than 72 hours before the first administration of the study drug.

Females of childbearing potential who

within 28 days before study entry, did not use a highly effective method of contraception, which includes any of the following:

total abstinence (if it is their preferred and usual lifestyle)*
an intrauterine device or intrauterine hormone-releasing system (IUS)
a contraceptive implant
an oral contraceptive (participant must be on a stable dose of the same oral contraceptive product for at least 28 days before dosing and throughout the study and for 90 days after study drug discontinuation)
have a vasectomized partner with confirmed azoospermia
do not agree to use a highly effective method of contraception (as described above) throughout the entire study period and for 90 days after study drug discontinuation.

For sites outside of the EU, it is permissible that if a highly effective method of contraception is not appropriate or acceptable to the participant, then the participant must agree to use a medically acceptable method of contraception, that is, double-barrier methods of contraception such as latex or synthetic condom plus diaphragm or cervical/vault cap with spermicide. NOTE: All females will be considered to be of childbearing potential unless they are postmenopausal (amenorrheic for at least 12 consecutive months, in the appropriate age group, and without other known or suspected cause) or have been sterilized surgically (that is, bilateral tubal ligation, total hysterectomy, or bilateral oophorectomy, all with surgery at least 1 month before dosing).

*Sexual abstinence is considered a highly effective method only if defined as refraining from heterosexual intercourse during the entire period of risk associated with the study intervention. The reliability of sexual abstinence needs to be evaluated in relation to the duration of the study and the preferred and usual lifestyle of the participant.

For Dose-Escalation only: Males who have not had a successful vasectomy (confirmed azoospermia) or they and their female partners do not meet the criteria above (that is, not of childbearing potential or practicing highly effective contraception throughout the study period and for 90 days after study drug discontinuation). If the female partner is pregnant, then males who do not agree to use latex or synthetic condoms throughout the study period and for 90 days after study drug discontinuation. No sperm donation is allowed during the study period and for 90 days after study drug discontinuation.
Pulmonary Function Test (PFT) abnormalities: FEV1/FVC <0.7, FEV1 or FVC <80%, DLCO <80%.
Current ILD/pneumonitis, or ILD/pneumonitis is suspected at Screening or history of interstitial lung disease (ILD)/pneumonitis of any severity including ILD/pneumonitis from prior anticancer therapy.
Current infectious pneumonia, history of viral pneumonia (including COVID-19-related infection) with evidence of persistent radiologic abnormalities.
Lung-specific clinically significant illnesses including, but not limited to any underlying pulmonary disorder (example, pulmonary embolism), asthma, chronic obstructive pulmonary disease (COPD), and restrictive lung disease.
Clinically significant pleural or pericardial effusion requiring drainage or ascites requiring peritoneal shunt.
Prior pneumonectomy.
History of chest radiotherapy. Participants with history of chest wall radiation (example, history of breast cancer) may be permitted if chest wall radiation is documented > 2 years before starting study treatment.
Any autoimmune, connective tissue, or inflammatory disorders (example, rheumatoid arthritis, Sjögren's syndrome, sarcoidosis, etc) where there is documented (or suspicion of) pulmonary involvement.
A known history of active TB (bacillus tuberculosis).
Scheduled for surgery during the study, other than minor surgery which would not delay study treatment.
An active clinically significant (in the opinion of the Investigator) infection requiring systemic therapy within 2 weeks prior to the first dose of study drug.
Administration of a live, attenuated vaccine within 4 weeks prior to the first dose of study drug, or anticipation that such a live attenuated vaccine will be required during the study. Inactivated vaccines (such as hepatitis A or polio vaccines) are permitted during the study. Seasonal influenza and COVID-19 vaccines that do not contain live virus are permitted.
Any prior hypersensitivity to monoclonal antibodies or contraindication to the receipt of corticosteroids or any of the excipients (investigators should refer to the prescribing information for the selected corticosteroid).
Known intolerance to either of the components of the study drug.
Any medical or other condition which, in the opinion of the investigator would preclude the participants participation in the clinical study.
Receiving any medication prohibited in combination with the study treatment(s) as described in the product label for eribulin, unless medication was stopped within 7 days prior to enrollment.
Known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial.

Study is for people with:

Breast Cancer

Phase:

Phase 1

Estimated Enrollment:

55

Study ID:

NCT04300556

Recruitment Status:

Recruiting

Sponsor:

Eisai Inc.

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There are 26 Locations for this study

See Locations Near You

Arizona Clinical Research Center - Hunt - PPDS
Tucson Arizona, 85715, United States
University of Arkansas For Medical Sciences
Little Rock Arkansas, 72205, United States
Stanford University School of Medicine
Stanford California, 94305, United States
H Lee Moffitt Cancer Center and Research Institute
Tampa Florida, 33612, United States
Winship Cancer Institute, Emory University
Atlanta Georgia, 30322, United States
Georgia Cancer Center at Augusta University
Augusta Georgia, 30912, United States
Northwestern University
Chicago Illinois, 60611, United States
Orchard Healthcare Research Inc
Skokie Illinois, 60077, United States
Johns Hopkins Sidney Kimmel Comprehensive Cancer Center
Baltimore Maryland, 21231, United States
Henry Ford Health System
Detroit Michigan, 48202, United States
MD Anderson Cancer Center at Cooper
Camden New Jersey, 08103, United States
Columbia University Medical Center
New York New York, 10032, United States
Memorial Sloan Kettering Cancer Center
New York New York, 11065, United States
University of Cincinnati Medical Center
Cincinnati Ohio, 45219, United States
Ohio State University
Columbus Ohio, 43210, United States
Oregon Health and Science University
Portland Oregon, 97239, United States
Chattanooga's Program In Women's Oncology
Chattanooga Tennessee, 37403, United States
University of Texas MD Anderson Cancer Center
Houston Texas, 77030, United States
University of Virginia Health System
Charlottesville Virginia, 22908, United States
Centre Antoine Lacassagne Centre Régional de Lutte Contre Le Cancer
Nice Alpes-Maritimes, 6100, France
ICANS - Institut de cancérologie Strasbourg Europe
Strasbourg Bas-Rhin, 67200, France
Clinique Catherine de Sienne
Nantes Loire-Atlantique, 44200, France
Centre Léon Bérard Centre Régional de Lutte Contre Le Cancer Rhône Alpes
Lyon Rhône, 69008, France
Beatson West of Scotland Cancer Centre - PPDS
Glasgow , G12 0, United Kingdom
Guys and St Thomas's Hospital
London , SE1 9, United Kingdom
The Christie NHS Foundation Trust - PPDS
Manchester , M20 4, United Kingdom

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Phase:

Phase 1

Estimated Enrollment:

55

Study ID:

NCT04300556

Recruitment Status:

Recruiting

Sponsor:


Eisai Inc.

How clear is this clinincal trial information?

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