Acute Myeloid Leukemia Clinical Trial

Study Comparing Blinatumomab Alternating With Low-intensity Chemotherapy Versus Standard of Care Chemotherapy for Older Adults With Newly Diagnosed Philadelphia-negative B-cell Precursor Acute Lymphoblastic Leukemia

Summary

The safety run-in part of the study aims to evaluate the safety and tolerability of blinatumomab alternating with low-intensity chemotherapy. The phase 3 part of the study aims to compare event-free survival (EFS) and overall survival (OS) of participants receiving blinatumomab alternating with low-intensity chemotherapy to EFS and (OS) of participants receiving standard of care (SOC) chemotherapy.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

- Age ≥ 55 years at the time of informed consent. OR

Age 40 to < 55 years of age if at least 1 of the following comorbidities at the time of informed consent:

history of grades 3 and 4 pancreatitis
diabetes mellitus with end-organ damage
severe liver disease such as cirrhosis stage 2 with portal hypertension or history of esophageal variceal bleeding and aspartate transaminase (AST)/alanine aminotransferase (ALT) > 10 x upper limit of normal (ULN) (liver cirrhosis must be confirmed by biopsy)
body mass index (BMI) ≥ 40 combined with relevant comorbidities such as metabolic syndrome

Any further combination of documented severe comorbidities that the investigator judges to be incompatible with administering an intensive pediatric based, adult adapted standard chemotherapy regimen but still compatible with the suggested protocol for older participants in both the experimental and the SOC arm. The participant history will be reviewed by the medical monitor during screening to determine enrollment acceptability based on a standard list with types of comorbidities allowed. A medical advisory board is available to the investigators for questions/advice and includes experts in the field of adult leukemia with experience with the use of blinatumomab, the global development lead for blinatumomab and the medical monitor of the study.

Participants with newly diagnosed Philadelphia (Ph)-negative B-cell precursor acute lymphoblastic leukemia (ALL)
Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2, higher ECOG score allowed if due to underlying leukemia
All participants must have adequate organ function as defined below:
renal: estimated glomerular filtration rate based on MDRD calculation ≥ 50 mL/min/1.73 m^2
liver function: total bilirubin ≤ 2x upper limit of normal (ULN; unless Gilbert's Disease or if liver involvement with leukemia); exception for participants 40 to < 55 years of age if they have a comorbidity listed above: severe liver disease such as cirrhosis stage 2 with portal hypertension or history of esophageal variceal bleeding and AST/ALT > 10 x ULN (liver cirrhosis must be confirmed by biopsy)
cardiac: left ventricular ejection fraction (LVEF) ≥ 50%

Exclusion Criteria:

Active central nervous system (CNS) leukemia not resolved with IT chemotherapy during screening.
Clinically relevant CNS pathology requiring treatment (eg, unstable epilepsy).
Current autoimmune disease or history of autoimmune disease with potential CNS involvement
Known infection with human immunodeficiency virus (HIV)
Known infection with chronic or active infection with hepatitis B (eg, hepatitis b surface [HBs] antigen reactive or quantifiable hepatitis b virus [HBV] viral load) or hepatitis C virus (HCV) (eg, HCV RNA [qualitative] is detected).

Active hepatitis B and C based on the following results:

positive for hepatitis B surface antigen (HepBsAg) (indicative of chronic hepatitis B or recent acute hepatitis B)
negative HepBsAg and positive for hepatitis B core antibody: negative HBV DNA by PCR result is necessary to enroll.

positive Hepatitis C virus antibody (HepCAb): negative hepatitis C virus RNA by PCR result is necessary to enroll.

Participant with symptoms and/or clinical signs and/or radiographic and/or sonographic signs that indicate an acute or uncontrolled chronic infection.
Cancer chemotherapy for this newly diagnosed B cell ALL before the start of protocol-required therapy with the exception of IT chemotherapy or pre-phase chemotherapy. Radiation to a spot lesion such as chloroma or lytic lesion of bone or vertebrae for pain or vertebral stabilization is allowed.

Study is for people with:

Acute Myeloid Leukemia

Phase:

Phase 3

Estimated Enrollment:

287

Study ID:

NCT04994717

Recruitment Status:

Recruiting

Sponsor:

Amgen

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There are 29 Locations for this study

See Locations Near You

City of Hope National Medical Center
Duarte California, 91010, United States
University of California at Irvine Medical Center
Orange California, 92868, United States
AdventHealth Orlando
Orlando Florida, 32804, United States
Saint Francis Hospital, Inc
Greenville South Carolina, 29607, United States
University of Texas MD Anderson Cancer Center
Houston Texas, 77030, United States
Princess Alexandra Hospital
Woolloongabba Queensland, 4102, Australia
Royal Adelaide Hospital
Adelaide South Australia, 5000, Australia
Peter MacCallum Cancer Centre
Melbourne Victoria, 3000, Australia
The Alfred Hospital
Melbourne Victoria, 3004, Australia
Fiona Stanley Hospital
Murdoch Western Australia, 6150, Australia
Charite Universitätsmedizin Berlin Campus Benjamin Franklin
Berlin , 12200, Germany
Universitätsklinikum Schleswig-Holstein
Kiel , 24105, Germany
Nagoya University Hospital
Nagoya-shi Aichi, 466-8, Japan
Akita University Hospital
Akita-shi Akita, 010-8, Japan
University of Fukui Hospital
Yoshida-gun Fukui, 910-1, Japan
Kyushu University Hospital
Fukuoka-shi Fukuoka, 812-8, Japan
Fukushima Medical University Hospital
Fukushima-shi Fukushima, 960-1, Japan
Sapporo Hokuyu Hospital
Sapporo-shi Hokkaido, 003-0, Japan
Tokai University Hospital
Isehara-shi Kanagawa, 259-1, Japan
Yokohama City University Medical Center
Yokohama-shi Kanagawa, 232-0, Japan
Nagasaki University Hospital
Nagasaki-shi Nagasaki, 852-8, Japan
National Hospital Organization Okayama Medical Center
Okayama-shi Okayama, 701-1, Japan
Osaka Metropolitan University Hospital
Osaka-shi Osaka, 545-8, Japan
Jichi Medical University Hospital
Shimotsuke-shi Tochigi, 329-0, Japan
Yamagata University Hospital
Yamagata-shi Yamagata, 990-9, Japan
Hospital Universitario Reina Sofia
Cordoba Andalucía, 14004, Spain
Hospital Universitario Virgen del Rocio
Sevilla Andalucía, 41013, Spain
Bagcilar Medipol Mega Universite Hastanesi
Istanbul , 34214, Turkey
Dokuz Eylul Universitesi Onkoloji Enstitusu
Izmir , 35340, Turkey

How clear is this clinincal trial information?

Study is for people with:

Acute Myeloid Leukemia

Phase:

Phase 3

Estimated Enrollment:

287

Study ID:

NCT04994717

Recruitment Status:

Recruiting

Sponsor:


Amgen

How clear is this clinincal trial information?

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