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A Safety and Tolerability Study of Peginesatide in Anemic Cancer Patients Receiving Cytotoxic Chemotherapy.

29. listopadu 2011 aktualizováno: Takeda

A Phase 1, Multicenter, Open-Label Dose Escalation Study Evaluating the Safety and Tolerability of Multiple Hematide Injections in Subjects With Refractory Non-Small Cell Lung Cancer, Breast Cancer, or Prostate Cancer Who Are Anemic and Receiving Cytotoxic Chemotherapy

The purpose of this study is to determine the safety and tolerability of peginesatide used to treat anemia in subjects diagnosed with recurrent non-small cell lung cancer, breast cancer or prostate cancer and who also receiving a taxane chemotherapy.

Přehled studie

Postavení

Ukončeno

Podmínky

Intervence / Léčba

Detailní popis

Currently approved erythropoiesis stimulating agents have been used successfully to increase hemoglobin levels, reduce fatigue and other anemia-related symptoms, improve daily function, and alleviate the need for transfusions of red blood cells in subjects with chronic kidney disease-related anemia or in cancer subjects with chemotherapy-induced anemia.

Peginesatide (hematide) Injection is a parenteral formulation for administration by intravenous or subcutaneous injection that is being developed for the correction of anemia in patients with chronic kidney disease, including patients on dialysis and patients not on dialysis, and for the treatment of patients with anemia due to concomitantly administered chemotherapy.

This is a multicenter, open-label dose escalation study to evaluate the safety, tolerability, and efficacy of multiple doses of peginesatide Injection in subjects with refractory non-small cell lung cancer, breast cancer, or prostate cancer. These subjects must have anemia diagnosed as a result of taxane chemotherapy.

Typ studie

Intervenční

Zápis (Aktuální)

2

Fáze

  • Fáze 1

Kontakty a umístění

Tato část poskytuje kontaktní údaje pro ty, kteří studii provádějí, a informace o tom, kde se tato studie provádí.

Studijní místa

    • Florida
      • Jacksonville, Florida, Spojené státy
    • Texas
      • Corpus Christi, Texas, Spojené státy

Kritéria účasti

Výzkumníci hledají lidi, kteří odpovídají určitému popisu, kterému se říká kritéria způsobilosti. Některé příklady těchto kritérií jsou celkový zdravotní stav osoby nebo předchozí léčba.

Kritéria způsobilosti

Věk způsobilý ke studiu

18 let až 80 let (Dospělý, Starší dospělý)

Přijímá zdravé dobrovolníky

Ne

Pohlaví způsobilá ke studiu

Všechno

Popis

Inclusion Criteria:

  • Females of childbearing potential who are sexually active must agree to use adequate contraception, and can neither be pregnant nor lactating from Screening throughout the duration of the study.
  • Individuals with one of the following histologically confirmed tumors:

    • stage IIIB/IV non-small-cell lung cancer
    • metastatic breast cancer
    • androgen insensitive prostate cancer and are scheduled to receive at least 4 weeks of chemotherapy, including a taxane.
  • Has progression or relapse after treatment with at least one regimen of chemotherapy or hormone therapy.
  • Has a hemoglobin value of greater than or equal to 8 and less than 10.5 g/dL within 1 week prior to administration of study drug.
  • Has an Eastern Cooperative Oncology Group Performance Status of 0-2.
  • Has one ferritin level greater than or equal to 100 ng/mL within 4 weeks prior to study drug administration.
  • Has one serum or red cell folate level above the lower limit of normal within 4 weeks prior to study drug administration.
  • Has one vitamin B12 level above the lower limit of normal within 4 weeks prior to study drug administration.
  • Has one absolute neutrophil count greater than or equal to 1.5 x 109/L within 1 week prior to administration of study drug.
  • The subject has a serum creatinine less than or equal to 1.5 mg/dL or a measured creatinine clearance greater than 60 mL/min.
  • The subject has one platelet count greater than or equal to 100 x 109/L within 1 week prior to administration of study drug.
  • The subject has a Life expectancy greater than 4 months.
  • The subject has a body mass index between 18 and 30 kg/m2, inclusive, prior to study drug administration.
  • The subject has a negative test result for hepatitis B surface antigen, and hepatitis C virus antibody at Screening.

Exclusion Criteria:

  • Has a history of failure to respond to erythropoiesis-stimulating agent treatment.
  • Has had treatment with any erythropoiesis-stimulating agent in the past 4 weeks.
  • Is known to have antibodies to other erythropoiesis-stimulating agents or history of Pure Red Cell Aplasia.
  • Has received Peginesatide in a previous clinical study or as a therapeutic agent.
  • Has a history of hypersensitivity or allergies to Peginesatide, other erythropoiesis-stimulating agents or related compounds.
  • Has had red blood cell transfusion within 4 weeks prior to study drug administration.
  • Has known hemoglobinopathy (eg, homozygous sickle-cell disease, thalassemia of all types, etc).
  • Has known hemolytic condition.
  • Has known blood loss as a cause of anemia, iron deficiency anemia, or anemia caused by gastrointestinal bleeding.
  • Has any previous or planned radiotherapy to more than 30% of active bone marrow.
  • Has donated more than 400 mL of blood within the 90 days preceding the beginning of the study.
  • Has known intolerance to parenteral iron supplementation.
  • Has received IV iron within 1 week of study drug administration.
  • Has history of bone marrow or peripheral blood cell transplantation.
  • Has central nervous system metastases.
  • Has a history of deep venous thrombosis, pulmonary embolism or other thrombotic event (eg, stroke, myocardial infarction, etc.) in the previous 6 months or known history of hypercoagulable disorder.
  • Has uncontrolled, or symptomatic inflammatory disease (eg, rheumatoid arthritis, systemic lupus erythematosus, etc).
  • Has poorly controlled hypertension per the investigator's judgment within 4 weeks prior to study drug administration (eg, systolic greater than or equal to 170 mm Hg or diastolic greater than or equal to 100 mm Hg on repeat readings).
  • Has had a seizure in the 6 months prior to study drug administration.
  • Has advanced chronic congestive heart failure - New York Heart Association Class III or IV.
  • Has a history or presence of an abnormal electrocardiogram at Screening that, in the investigator's opinion, is clinically significant.
  • Has a known history of human immunodeficiency virus.
  • Has a history of drug abuse (defined as any illicit drug use) or a history of alcohol abuse (defined as consumption of more than 4 alcoholic drinks per day) within 1 year prior to Baseline.
  • Has aspartate aminotransferase or alanine aminotransferase greater than 2.5 times the upper limit of normal (aspartate aminotransferase or alanine aminotransferase greater than 5 times the upper limit of normal if liver metastases are present), active liver disease or jaundice.
  • Is currently taking or anticipated to require anticoagulants other than aspirin (eg, coumadin, ticlopidine, etc.).
  • Has a bilirubin greater than the upper limit of normal.
  • Has pyrexia/fever greater than or equal to 39°C within 48 hours prior to study drug administration.
  • Has high likelihood of early withdrawal or interruption of the study (eg, myocardial infarction within the past 3 months, severe or unstable coronary artery disease, stroke, respiratory, autoimmune, neuropsychiatric or neurological abnormalities, or any other clinically significant medical diseases or conditions within the prior 6 months that may, in the investigator's opinion, interfere with assessment or follow-up of the subject).
  • Has anticipated elective surgery during the study period.
  • Has exposure to any investigational agent within 1 month prior to administration of study drug or planned receipt during the study period.

Studijní plán

Tato část poskytuje podrobnosti o studijním plánu, včetně toho, jak je studie navržena a co studie měří.

Jak je studie koncipována?

Detaily designu

  • Primární účel: Léčba
  • Přidělení: N/A
  • Intervenční model: Přiřazení jedné skupiny
  • Maskování: Žádné (otevřený štítek)

Zbraně a zásahy

Skupina účastníků / Arm
Intervence / Léčba
Experimentální: Peginesatid

Peginesatide 0.075, 0.1, 0.125, 0.15, 0.175, 0.2, 0.225 or 0.25 mg/kg administered subcutaneously every 3 weeks for a total of at least 2 doses. Subsequent injections given every 3 weeks thereafter regardless of the schedule of subsequent chemotherapy cycles.

Following Study Day 43, subjects may continue on Peginesatide treatment, dosing every 3 weeks until 4 weeks after discontinuation of taxane-containing chemotherapy regimen, the occurrence of a dose limiting toxicity, documented disease progression or change in chemotherapy regimen.

Ostatní jména:
  • Hematid

Co je měření studie?

Primární výstupní opatření

Měření výsledku
Časové okno
Maximum tolerated dose.
Časové okno: End of Treatment.
End of Treatment.

Sekundární výstupní opatření

Měření výsledku
Časové okno
Proportion of subjects who have 2 consecutive Hgb values of either an increase of ≥1 g/dL or a Hgb ≥11 g/dL in the absence of a red blood cell transfusion.
Časové okno: At All Visits for every cycle.
At All Visits for every cycle.
Proportion of subjects who have an increase in Hgb of ≥1 g/dL or a Hgb ≥11 g/dL in the absence of a red blood cell transfusion.
Časové okno: Days 22 and 43 for every cycle.
Days 22 and 43 for every cycle.
Proportion of subjects with 2 consecutive Hgb values increase of ≥1 g/dL or ≥11 g/dL during the Treatment phase absent of red blood cell transfusion within the prior 28 days and without excursion of Hgb values above 12 g/dL for ≥2 consecutive weeks.
Časové okno: Within the prior 28 days of every cycle for a minimum of 2 consecutive weeks.
Within the prior 28 days of every cycle for a minimum of 2 consecutive weeks.
Proportion of subjects who received at least 1 RBC transfusion.
Časové okno: From Day 29 to End of Treatment for every cycle.
From Day 29 to End of Treatment for every cycle.
Change from Baseline in Hemoglobin.
Časové okno: At Each Visit for every cycle.
At Each Visit for every cycle.
Duration of maintaining Hgb values within the range of 10.5 g/dL and 12.0 g/dL.
Časové okno: At Each Visit for every cycle.
At Each Visit for every cycle.
Pharmacokinetics of Peginesatide (PK Cohort Only).
Časové okno: At Each Visit for every cycle.
At Each Visit for every cycle.
Adverse events and serious adverse events.
Časové okno: At All Visits for every cycle.
At All Visits for every cycle.
Physical examination (including weight, vital signs, and oral temperature).
Časové okno: At All Visits for every cycle.
At All Visits for every cycle.
Clinical Laboratory Tests and Electrocardiograms.
Časové okno: At All Visits for every cycle.
At All Visits for every cycle.
Electrocardiograms.
Časové okno: At Final Visit for every cycle.
At Final Visit for every cycle.
Signs and symptoms for thromboembolytic events.
Časové okno: At All Visits for every cycle.
At All Visits for every cycle.
Proportion of subjects who have incidence of Hgb values >12 g/dL.
Časové okno: At All Visits for every cycle.
At All Visits for every cycle.
Proportion of subjects who have Hgb increases by more than 1 g/dL in a 2-week period.
Časové okno: At All Visits for every cycle.
At All Visits for every cycle.
Tumor progression.
Časové okno: Every 2 cycles of chemotherapy.
Every 2 cycles of chemotherapy.

Spolupracovníci a vyšetřovatelé

Zde najdete lidi a organizace zapojené do této studie.

Sponzor

Spolupracovníci

Vyšetřovatelé

  • Ředitel studie: Vice President Clinical Science, Takeda

Termíny studijních záznamů

Tato data sledují průběh záznamů studie a předkládání souhrnných výsledků na ClinicalTrials.gov. Záznamy ze studií a hlášené výsledky jsou před zveřejněním na veřejné webové stránce přezkoumány Národní lékařskou knihovnou (NLM), aby se ujistily, že splňují specifické standardy kontroly kvality.

Hlavní termíny studia

Začátek studia

1. ledna 2008

Primární dokončení (Aktuální)

1. června 2008

Dokončení studie (Aktuální)

1. června 2008

Termíny zápisu do studia

První předloženo

26. února 2008

První předloženo, které splnilo kritéria kontroly kvality

5. března 2008

První zveřejněno (Odhad)

6. března 2008

Aktualizace studijních záznamů

Poslední zveřejněná aktualizace (Odhad)

1. prosince 2011

Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality

29. listopadu 2011

Naposledy ověřeno

1. listopadu 2011

Více informací

Termíny související s touto studií

Klíčová slova

Další identifikační čísla studie

  • HEM_101
  • U1111-1126-1765 (Identifikátor registru: WHO)

Tyto informace byly beze změn načteny přímo z webu clinicaltrials.gov. Máte-li jakékoli požadavky na změnu, odstranění nebo aktualizaci podrobností studie, kontaktujte prosím register@clinicaltrials.gov. Jakmile bude změna implementována na clinicaltrials.gov, bude automaticky aktualizována i na našem webu .

Klinické studie na Peginesatide

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