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Terminated/Withdrawn
Astellas Study ID
1235-CL-0101

A Study to Evaluate Escalating Doses of ASP1235 (AGS62P1) Given as Monotherapy in Subjects with Acute Myeloid Leukemia (AML)

Astellas Study ID
1235-CL-0101
Clinicaltrials.gov ID
NCT02864290
EUCTIS ID
N/A
EudraCT ID
N/A
jRCT ID
N/A
CN CDE ID
N/A
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Study summary

The purpose of this study is to evaluate the safety and tolerability of ASP1235 (AGS62P1) given at three dosing schedules (Schedule A, every three weeks [Q3W] or Schedule B, every other week of a 4 week cycle [Q2W] or Schedule C once a week for 3 weeks of a 4 week cycle) in subjects with acute myeloid leukemia (AML) and determine the maximum tolerated dose (MTD). In addition, this study will assess the pharmacokinetics (PK), the immunogenicity and the anti-leukemic activity of ASP1235 (AGS62P1).

Additional Study Details

Phase
Phase 1
Product
ASP1235
Product
ASP1235
Type
Interventional
Masking
None (Open Label)
Enrollment number
43
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Study documents

Scientific Results Summary
Available Language(s): English
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Plain Language Summary
Available Language(s): English
Download Document(s)

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Would you like more information about clinical trial sites that are recruiting participants for A Study to Evaluate Escalating Doses of ASP1235 (AGS62P1) Given as Monotherapy in Subjects with Acute Myeloid Leukemia (AML)? Contact us by filling out your information to the right and we’ll respond to you.

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  • Algeria
  • Argentina
  • Armenia
  • Australia
  • Austria
  • Belarus
  • Belgium
  • Bosnia And Herzegovina
  • Brazil
  • Bulgaria
  • Canada
  • Chile
  • China
  • Colombia
  • Croatia
  • Czech Republic
  • Denmark
  • Dominican Republic
  • Egypt
  • Estonia
  • Finland
  • Former Serbia and Montenegro
  • France
  • Georgia
  • Germany
  • Greece
  • Guatemala
  • Hong Kong
  • Hungary
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  • India
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  • Ireland
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  • Latvia
  • Lebanon
  • Lithuania
  • Macedonia
  • Malaysia
  • Mexico
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  • Peru
  • Philippines
  • Poland
  • Portugal
  • Puerto Rico
  • Republic of Korea
  • Republic of Moldova
  • Romania
  • Russian Federation
  • Saudi Arabia
  • Serbia
  • Singapore
  • Slovakia
  • Slovenia
  • South Africa
  • Spain
  • Sweden
  • Switzerland
  • Taiwan, Province of China
  • Thailand
  • Turkey
  • Ukraine
  • United Kingdom
  • United States
  • Vietnam

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    Locations

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    Terminated (Halted Prematurely)
    Site US00001
    Houston, TX, United States, 77030
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    Terminated (Halted Prematurely)
    Site US00003
    Baltimore, MD, United States, 21287
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    Completed
    Site US00006
    Duarte, CA, United States, 91010
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    Completed
    Site CA00010
    Toronto, ON, Canada, M5G 2M9
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    Completed
    Site US00007
    Boston, MA, United States, 02114
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    Completed
    Site US00009
    Boston, MA, United States, 02114
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    Completed
    Site US00004
    New York, NY, United States, 10016
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    Trial info
    Follow Trial
    Age
    18+ years
    Diamond icon
    Condition
  • Leukemia - AML
    • Gender icon
    Sex
    Female & Male
    Calendar icon
    Trial Dates
    Nov 2016 - Sep 2020
    Additional Study Details
    Inclusion Criteria
    • Subject has morphologically documented primary or secondary AML by the World Health Organization (WHO) criteria (2008) which is relapsed or refractory after failing at least 1 regimen and is not a candidate for established salvage treatment regimens. For expansion cohorts, patients are eligible if they have had ≤ 3 prior lines of therapy. Lines of therapy include initial induction (up to 2 cycles) with consolidation/maintenance, if applicable, and subsequent salvage regimens. Consolidation alone and stem cell transplantation are not counted as lines of therapy.
    • Subject has an Eastern Cooperative Oncology Group performance score (ECOG) ≤ 2
    • Subject has adequate renal function with an estimated creatinine clearance of ≥ 30 mL/min by the Cockcroft-Gault equation adjusted for body weight
    • Subject has a total bilirubin ≤ 1.5 x upper limit of normal (ULN), albumin ≥ 2.5 g/d, aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 2.5 x upper limit of normal (ULN)
    • Subjects must be competent to comprehend, provide written informed consent, and date an independent ethics committee/institutional review board/research ethics board (IEC/IRB/REB) approved informed consent form
    • A female subject is eligible to participate if she is not pregnant and at least one of the following conditions applies:
      • Not a woman of childbearing potential (WOCBP) OR
      • WOCBP who agrees to follow the contraceptive guidance throughout the treatment period and for at least 6 months after the final study drug administration.
    • Female subject must agree not to breastfeed starting at screening and throughout the study period, and for 6 months after the final study drug administration.
    • Female subject must not donate ova starting at screening and throughout the study period, and for 6 months after the final study drug administration.
    • A male subject with female partner(s) of child-bearing potential must agree to use contraception during the treatment period and for at least 6 months after the final study drug administration.
    • A male subject must not donate sperm during the treatment period and for at least 6 months after the final study drug administration.
    • Male subject with a pregnant or breastfeeding partner(s) must agree to remain abstinent or use a condom for the duration of the pregnancy or time partner is breastfeeding throughout the study period and for 6 months after the final study drug administration.
    MaximizeExclusion Criteria
    • Subject has a diagnosis of acute promyelocytic leukemia (APL)
    • Subject has preexisting sensory or motor neuropathy Grade ≥ 2 at baseline
    • Subject has received small molecule therapy, radiotherapy, immunotherapy, monoclonal antibodies, investigational drug, or chemotherapy within 14 days before first dose of study drug, with the exception of hydroxyurea
    • Subject has any Grade ≥ 2 persistent non-hematological toxicity related to allotransplant
    • Subject with Graft vs. Host Disease (GVHD) who is receiving treatment with systemic glucocorticoids > 10 mg/day equivalent of prednisone; however, treatment with low dose glucocorticoids (≤ 10 mg/day equivalent of prednisone) is permitted
      • The use of systemic glucocorticoids in excess of 10 mg/day equivalent of prednisone is permitted provided it is not for the treatment of GVHD (e.g. chronic obstructive pulmonary disease, anti-emetic, infusion reactions). The chronic use of topical, inhaled, and locally injected steroids is permitted
    • Subject has known current central nervous system (CNS) disease
    • Active angina or Class III or IV Congestive Heart Failure (CHF) (New York Heart Association CHF Functional Classification System) or clinically significant cardiac disease within 12 months of the first dose of study drug, including myocardial infarction, unstable angina, Grade 2 or greater peripheral vascular disease, congestive heart failure, uncontrolled hypertension, or arrhythmias not controlled by medication
    • Subject has clinical evidence of Disseminated Intravascular Coagulation
    • Subject has known positivity for human immunodeficiency virus
    • Subject has known active hepatitis B (positive hepatitis B surface antigen [HBs Ag]) or C infection. For subjects who are negative for HBs Ag, but hepatitis B core antibody (HBc Ab) positive, an HB deoxyribonucleic acid (DNA) test will be performed and if positive, the subject will be excluded. Subjects with positive serology but negative hepatitis C virus (HCV) ribonucleic acid (RNA) test results are eligible.
    • Subject has an uncontrolled active infection requiring treatment and grade 3 or higher fever 48 hours before the first dose of study drug. Controlled infections (i.e. 3 negative cultures completing antibiotics and/or stable fungal infection in therapy) are allowed provided the subject has a temperature of < 38.3°C within 48 hours of the first dose of study drug.
    • Subject has a known sensitivity to any of the components of the investigational product ASP1235 (AGS62P1):
      • ASP1235 (AGS62P1)
      • L-Histidine base
      • L-Histidine HCl
      • α, α -Trehalose Dihydrate
      • Polysorbate 20
    • Major surgery within 28 days of the first dose of study drug
    • Subject is pregnant or lactating
    • Subject has a condition or situation which may put the subject at significant risk, may confound the study results, or may interfere significantly with subject's participation in the study
    • Subject has any medical, psychiatric, addictive or other disorder which compromises the ability of the subject to give written informed consent and/or to comply with procedures
    • Subject has ocular condition such as:
      • Active infection or corneal ulcer
      • Monocularity
      • History of corneal transplantation
      • Contact lens dependent (if using contact lens, must be able to switch to glasses during the entire study duration)
      • Uncontrolled glaucoma (topical medications allowed)
      • Uncontrolled or active ocular problems (e.g., retinopathy, macular edema, active uveitis, macular degeneration) requiring surgery, laser treatment, or intravitreal injections
      • Papilledema or other active optic nerve disorder

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