Efficacy and Safety of KD025 in Subjects With cGVHD After At Least 2 Prior Lines of Systemic Therapy



Status:Recruiting
Conditions:Hematology
Therapuetic Areas:Hematology
Healthy:No
Age Range:18 - Any
Updated:3/30/2019
Start Date:October 15, 2018
End Date:January 2022

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A Phase 2, Randomized, Multicenter Study to Evaluate the Efficacy and Safety of KD025 in Subjects With Chronic Graft Versus Host Disease (cGVHD) After At Least 2 Prior Lines of Systemic Therapy (The ROCKstar Study)

This is a Phase 2, randomized, multicenter study to evaluate the efficacy and safety of KD025
in subjects with Chronic Graft Versus Host Disease (cGVHD) after at least 2 prior lines of
systemic therapy

Phase 2, open label, randomized, multicenter study in subjects with cGVHD who have previously
been treated with at least 2 prior lines of systemic therapy. Approximately 126 subjects with
active cGVHD will be randomized (1:1) to receive treatment with one of two KD025 regimens:

- Arm A: KD025 200mg QD

- Arm B: KD025 200mg BID

Randomization will be stratified according to prior cGVHD treatment with ibrutinib (Yes / No)
and severe cGVHD at baseline (Yes / No). Subjects may receive treatment in 28-day treatment
cycles until progression of cGVHD. Subjects who have not achieved a response after 12 cycles
of KD025 should be withdrawn if in the Investigator's judgment there is no evidence of
clinical benefit. Subjects will undergo evaluations as outlined in the Study Assessments
table. The primary endpoint is the overall response rate (ORR) with responses as defined by
the 2014 National Institute of Health (NIH) Consensus Development Project on clinical trials
in cGVHD.

Inclusion Criteria:

1. Adult male and female subjects at least 18 years of age who have had allogenic
hematopoietic cell transplant (HCT).

2. Previously received at least 2 and not more than 5 lines of systemic therapy for cGVHD

3. Receiving glucocorticoid therapy with a stable dose over the 2 weeks prior to
screening

4. Have persistent cGVHD manifestations and systemic therapy is indicated

5. Karnofsky Performance Score of ≥ 60

Exclusion Criteria:

1. Received a systemic investigational cGVHD treatment within 28 days of study entry.
Prior treatment is allowed with a washout of at least 5 half-lives or 28 days. (Note:
Corticosteroids, calcineurin inhibitors, sirolimus, MMF, methotrexate and ECP are
acceptable and subjects must have been on a stable dose / regimen of these for at
least 2 weeks prior to screening).

2. Histological relapse of the underlying cancer or post-transplant lymphoproliferative
disease at the time of screening.

3. Current treatment with ibrutinib. Prior treatment with ibrutinib is allowed with a
washout of at least 28 days prior to randomization.
We found this trial at
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Los Angeles, California 90095
310-825-4321
Phone: 310-794-0242
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1648 Pierce Dr NE
Atlanta, Georgia 30322
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185 Cambridge Street
Boston, Massachusetts 02114
617-724-5200
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4100 John R
Detroit, Michigan 48201
800-527-6266
Phone: 313-576-9271
Barbara Ann Karmanos Cancer Institute Karmanos is based in southeast Michigan, in midtown Detroit, and...
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101 Jessup Hall
Iowa City, Iowa 52242
(319) 335-3500
Phone: 319-356-8133
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Minneapolis, Minnesota 55455
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Phone: 612-624-0123
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1211 Medical Center Dr
Nashville, Tennessee 37232
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60 Crittenden Blvd # 70
Rochester, New York 14642
(585) 275-2121
Phone: 585-275-5345
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12902 USF Magnolia Dr
Tampa, Florida 33612
(888) 663-3488
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H. Lee Moffitt Cancer Center & Research Institute Moffitt Cancer Center in Tampa, Florida, has...
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Augusta, Georgia 30912
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901 West Ben White Boulevard
Austin, Texas 78704
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450 Brookline Ave
Boston, Massachusetts 2215
617-632-3000
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1721 East 19th Ave., Suite #200 & #300
Denver, Colorado 80218
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1500 East Duarte Road
Duarte, California 91010
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Fairway, Kansas 66205
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1515 Holcombe Blvd
Houston, Texas 77030
 713-792-2121
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Milwaukee, Wisconsin
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Nashville, Tennessee 37203
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