Trilaciclib (G1T28), a CDK 4/6 Inhibitor, in Combination With Etoposide and Carboplatin in Extensive Stage Small Cell Lung Cancer (SCLC)



Status:Active, not recruiting
Conditions:Lung Cancer, Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - Any
Updated:11/18/2018
Start Date:June 26, 2015
End Date:January 2020

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Phase 1b/2a Safety and Pharmacokinetic Study of G1T28 in Patients With Extensive Stage Small Cell Lung Cancer (SCLC) Receiving Etoposide and Carboplatin

This is a study to investigate the potential clinical benefit of trilaciclib (G1T28) in
preserving the bone marrow and the immune system, and enhancing chemotherapy antitumor
efficacy when administered prior to carboplatin and etoposide in first line treatment for
patients with newly diagnosed extensive-stage SCLC.

The study consists of 2 parts: a limited open-label, dose-finding portion (Part 1), and a
randomized double-blind portion (Part 2). Both parts include 3 study phases: Screening Phase,
Treatment Phase, and Survival Follow-up Phase. The Treatment Phase begins on the day of first
dose with study treatment and completes at the Post-Treatment Visit. Approximately, 90
patients will be enrolled in the study; 20 patients in the Part 1 and 70 patients in the Part
2 portion.


Inclusion Criteria:

- Male or female subjects aged ≥18 years

- Unequivocally confirmed diagnosis of SCLC by histology or cytology, preferably
including the presence of neuroendocrine features by immunohistochemistry

- At least 1 target lesion that is unirradiated and measurable by RECIST, Version 1.1

- Eastern Cooperative Oncology Group (ECOG) performance status of 0 - 2

- Adequate organ function

Exclusion Criteria:

- Prior chemotherapy for extensive-stage SCLC

- Presence of symptomatic brain metastases requiring immediate treatment with radiation
therapy or steroids.

- Uncontrolled ischemic heart disease or uncontrolled symptomatic congestive heart
failure

- Known history of stroke or cerebrovascular accident within 6 months prior to
enrollment

- Other uncontrolled serious chronic disease or conditions that in the investigator's
opinion could affect compliance or follow-up in the protocol

- Concurrent radiotherapy to any site or radiotherapy within 2 weeks prior to enrollment
or previous radiotherapy to the target lesion sites (the sites that are to be followed
for determination of a response)

- Receipt of any investigational medication within 4 weeks prior to enrollment
We found this trial at
27
sites
Knoxville, Tennessee 37920
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201 Dowman Dr
Atlanta, Georgia 30303
(404) 727-6123
Principal Investigator: Taofeek Owonikoko, MD
Phone: 404-778-1842
Emory University Emory University, recognized internationally for its outstanding liberal artscolleges, graduate and professional schools,...
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Atlanta, GA
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Albuquerque, New Mexico 87131
Principal Investigator: Vi Chiu, MD
Phone: 505-925-0654
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Athens, Georgia 30607
Principal Investigator: Petros Nikolanikos, MD
Phone: 706-353-2990
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Athens, GA
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6410 Rockledge Dr #660
Bethesda, Maryland 20817
(301) 571-0019
Principal Investigator: Ralph Boccia, MD
Phone: 301-571-2016
Center for Cancer & Blood Disorders Widely recognized for its compassionate, expert care, the Center...
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Boca Raton, Florida 33486
Principal Investigator: Edgardo Santos, MD
Phone: 561-955-4539
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Boca Raton, FL
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Buffalo, New York 14263
Principal Investigator: Hongbin Chen, MD
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Buffalo, NY
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Chapel Hill, North Carolina 27599
Principal Investigator: Jared Weiss, MD
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Colorado Springs, Colorado 80909
Principal Investigator: Robert Hoyer, MD
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2121 East Harmony Road
Fort Collins, Colorado 80528
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Fort Myers, Florida 33916
Principal Investigator: Lowell Hart, MD
Phone: 239-274-8200
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Greenville, South Carolina 29615
Principal Investigator: Jeff Edenfield, MD
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Hot Springs, Arkansas 71913
Principal Investigator: R. Timothy Webb, MD
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Knoxville, Tennessee 37920
Principal Investigator: Wahid Hanna, MD
Phone: 865-305-9773
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Lebanon, New Hampshire 03756
Principal Investigator: Konstantin Dragnev, MD
Phone: 603-650-4428
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Louisville, Kentucky 40207
Principal Investigator: John Hamm, MD
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Oklahoma City, Oklahoma 73117
Principal Investigator: Raid Aljumaily, MD
Phone: 405-271-8001
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1020 Walnut St
Philadelphia, Pennsylvania 19107
(215) 955-6000
Phone: 215-955-1964
Thomas Jefferson University We are dedicated to the health sciences and committed to educating professionals,...
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Rennes,
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Rogers, Arkansas 72758
Principal Investigator: Thaddeus Beck, MD
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Sayre, Pennsylvania 18840
Principal Investigator: Bradley Lash, MD
Phone: 570-887-2141
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Spartanburg, South Carolina 29303
Principal Investigator: Caio Rocha-Lima, MD
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Tavares, Florida 32778
Principal Investigator: Maen Hussein, MD
Phone: 727-216-1143
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Tyler, Texas 75702
Principal Investigator: Donald Richards, MD
Phone: 903-579-9800
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Tyler, TX
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Vancouver, Washington 98684
Principal Investigator: David Smith, MD
Phone: 360-449-6522
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Vancouver, WA
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West Palm Beach, Florida 33401
Principal Investigator: Todd Gersten, MD
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Whittier, California 90606
Principal Investigator: Richy Agajanian, MD
Phone: 562-693-2299
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