- ICH GCP
- Rejestr badań klinicznych w USA
- Badanie kliniczne NCT01204164
Phase 1 Study of TG02 Citrate in Patients With Advanced Hematological Malignancies (TG02-101)
Phase 1 Dose-Escalation and Pharmacokinetic Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Przegląd badań
Status
Warunki
Interwencja / Leczenie
Szczegółowy opis
This is a multicenter, open-label, dose escalation, Phase 1/1b study.
For Parts 1, 2, and 3 of the study, the primary objective is to determine the highest dose of TG02 citrate that can safely be given to patients with different types of hematological malignancy.
For Part 4, the primary objective is to evaluate the safety and tolerability of once-weekly dosing at the maximum-tolerated dose/ Recommended Phase 2 Dose of TG02 in combination with carfilzomib.
This study consists of four parts:
- Part 1: single agent TG02 in acute leukemia patients
- Part 2: single agent TG02 in multiple myeloma patients
- Part 3: TG02 in combination with carfilzomib in multiple myeloma patients
- Part 4: TG02 in combination with carfilzomib in carfilzomib refractory multiple myeloma patients.
Typ studiów
Zapisy (Oczekiwany)
Faza
- Faza 1
Kontakty i lokalizacje
Lokalizacje studiów
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Colorado
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Denver, Colorado, Stany Zjednoczone, 80218
- RMCC
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Georgia
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Atlanta, Georgia, Stany Zjednoczone, 30322
- EMORY
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Illinois
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Chicago, Illinois, Stany Zjednoczone, 60612
- Rush
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Indiana
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Indianapolis, Indiana, Stany Zjednoczone, 46202
- IU
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New Jersey
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Hackensack, New Jersey, Stany Zjednoczone, 07601
- HUMC
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New York
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New York City, New York, Stany Zjednoczone, 10021
- Cornell
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Ohio
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Columbus, Ohio, Stany Zjednoczone, 43210
- OSU
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Tennessee
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Nashville, Tennessee, Stany Zjednoczone, 37203
- SCRI
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Texas
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Houston, Texas, Stany Zjednoczone, 77030
- MDACC
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Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
Akceptuje zdrowych ochotników
Płeć kwalifikująca się do nauki
Opis
Part 1 Inclusion Criteria:
- Relapsed AML, ALL, CML in blast crisis, or MDS
- 65+ yrs with AML not eligible for standard frontline chemo
- Interval from prior treatment to time of study drug at least 5 half-lives for cytotoxic/ noncytotoxic agents.
- Persistent clinically significant toxicities from prior chemo ≤ Grd 1
- ECOG PS 0-2
Lab values:
- Cr ≤ 2X ULN
- ALT and/or AST ≤2.5 X ULN
- Total bilirubin ≤1.5 X ULN unless considered due to Gilbert's syndrome
- Negative pregnancy test
- Can take oral med
Part 2 Inclusion Criteria:
- Relapsed multiple myeloma. At least ≥1 line of therapy and progressed after ≥1 prior therapy
Measurable disease defined as at least one of the following:
- Serum M ≥500 mg/dL
- Urine M ≥200 mg per 24hr
- Involved FLC ≥10 mg/dL and abnormal FLC ratio in serum (<0.26 or >1.65)
- Measurable soft tissue plasmacytoma
- Persistent clinically significant toxicities from prior chemo ≤ Grd 1
- ECOG PS 0-2
Lab values:
- ANC of >1000/mm3
- Platelets ≥50,000/mm3
- Cr ≤2X the ULN
- ALT and/or AST ≤2.5X ULN
- Total bilirubin ≤1.5X ULN, unless considered due to Gilbert's syndrome
- Negative pregnancy test
- Can take oral med
Part 3 Inclusion Criteria:
Measurable disease defined as at least one of the following:
- Serum M ≥500 mg/dL
- Urine M protein ≥200 mg per 24hr
- Involved FLC level ≥10 mg/dL and abnormal FLC ratio in serum (<0.26 or >1.65)
Meet at least one of the criteria below:
- a. ≥2 prior therapies including proteasome inhibitor and immunomodulatory agent (IMiD)
- b. ≥1 prior therapy and one of the following abnormalities: 17p del, p53, 1q amp, 1p del, t(4;14)
- Interval from prior treatment to time of study drug at least 5 half-lives or 3 wks, which ever is shorter, for noncytotoxic agents
- Persistent clinically significant toxicities from prior chemo ≤ Grd 1 or Grd 2 neuropathy without pain
- ECOG PS 0-2
Lab values:
- ANC of >1000/mm3 independent of G-CSF
- Platelets ≥50,000/mm3 independent of transfusion
- MDRD calculated or measured CrCl of ≥30 mL/min
- ALT and/or AST ≤3X ULN
- Total bilirubin ≤2X ULN, unless considered due to Gilbert's syndrome
- Negative pregnancy test
- Can take oral med
Part 4 Inclusion Criteria:
Measurable disease defined as at least one of the following:
- Serum M ≥500 mg/dL
- Urine M protein ≥200 mg per 24hr
- Involved FLC level ≥10 mg/dL and an abnormal FLC ratio in serum (<0.26 or >1.65)
Received prior therapies including:
- a. bortezomib
- b. an IMiD
- c. carfilzomib. Demonstrated disease progression on or within 60d of completion of carfilzomib therapy
- Interval from prior treatment to time of study drug at least 5 half-lives or 3 wks, which ever is shorter, for noncytotoxic agents.
- Persistent clinically significant toxicities from prior chemo ≤ Grd 1, or Grd 2 neuropathy without pain.
- ECOG PS 0-2
Lab values:
- ANC of >1000/mm3 independent of G-CSF
- Platelets ≥50,000/mm3 independent of transfusion
- MDRD calculated or measured CrCl of ≥30 mL/min
- ALT and/or AST ≤3X ULN
- Total bilirubin ≤2X ULN, unless considered due to Gilbert's syndrome
- Negative pregnancy test
- Can take oral med
Parts 1 and 2 Exclusion Criteria:
- Previous allogenic hematopoietic transplant within 90 d
- Concurrent severe or uncontrolled medical disease that would compromise the safety or compromise the ability of the patient to complete the study
- Prolonged QTC interval >450ms
- Symptomatic CNS metastases
- Known HIV or AIDS
- Actively treated for a second malignancy
- Pregnant or nursing women
Part 3 Exclusion Criteria:
- Multiple myeloma of IgM subtype, POEMS, plasma cell leukemia
- Corticosteroids discontinued ≥7 days of initiating therapy
- Previous chemo within 2 wks
- Hx of ventricular arrhythmia or symptomatic conduction abnormality within 12m
- CHF, symptomatic ischemia, conduction abnormalities uncontrolled by conventional intervention, myocardial infarction within 6m
- Prolonged QTc interval (males >450ms, females >470ms)
- Previous allogeneic hematopoietic transplant within 90 days of study enrollment, Active GVHD requiring treatment.
- Concurrent severe or uncontrolled medical disease that would compromise the safety or compromise the ability of the patient to complete the study
- Symptomatic CNS metastases
- Known HIV or AIDS
- Prior or 2nd malignancy, except non-melanoma skin cancer, completely resected cervical or prostate cancer (with PSA of less than or equal to 0.1 ng/ml), or other cancer for which the subject has received curative therapy at least 3 yrs prior to study entry
- Treatment-related MDS
- Significant neuropathy (Grd 3-4 or Grd 2 with pain) at the time of 1st dose
- Primary AL amyloidosis
- Pleural effusions requiring thoracentesis or ascites requiring paracentesis
- Pregnant or nursing women
Part 4 Exclusion Criteria:
- Multiple myeloma of IgM subtype, POEMS, plasma cell leukemia
- Previous chemo within 2 wks
- Hx ventricular arrhythmia or symptomatic conduction abnormality within 12m
- CHF, symptomatic ischemia, conduction abnormalities uncontrolled by conventional intervention, and myocardial infarction within 6m
- Prolonged QTc interval (males >450ms, females >470ms)
- Previous allogeneic hematopoietic transplant within 90 days. Active GVHD requiring treatment
- Concurrent severe or uncontrolled medical disease that would compromise the safety or compromise the ability of the patient to complete study
- Symptomatic CNS metastases
- Known HIV or AIDS
- Prior or 2nd malignancy, except non-melanoma skin cancer, completely resected cervical or prostate cancer (with PSA of less than or equal to 0.1 ng/ml), or other cancer for which the subject has received curative therapy at least 3 yrs prior to study entry
- Treatment-related MDS
- Significant neuropathy (Grd 3-4 or Grd 2 with pain) at the time of 1st dose
- Primary AL amyloidosis
- Pleural effusions requiring thoracentesis or ascites requiring paracentesis
- Pregnant or nursing women
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie
- Przydział: Nielosowe
- Model interwencyjny: Zadanie dla jednej grupy
- Maskowanie: Brak (otwarta etykieta)
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
|---|---|
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Eksperymentalny: TG02 in AL
Single agent TG02 citrate in acute leukemia patients
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TG02 citrate capsules given orally.
Inne nazwy:
|
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Eksperymentalny: TG02 in MM
Single Agent TG02 citrate in multiple myeloma patients
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TG02 citrate capsules given orally.
Inne nazwy:
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Eksperymentalny: TG02 + CFZ in MM
TG02 in combination with carfilzomib and dexamethasone in multiple myeloma patients
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TG02 citrate capsules given orally.
Inne nazwy:
Carfilzomib per PI
Inne nazwy:
|
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Eksperymentalny: TG02 + CFZ + DEX in CFZ refractory MM
TG02 in combination with carfilzomib and dexamethasone in carfilzomib refractory multiple myeloma patients
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TG02 citrate capsules given orally.
Inne nazwy:
Carfilzomib per PI
Inne nazwy:
Dexamethasone (Oral or IV)
Inne nazwy:
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Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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Maximum Tolerated Dose
Ramy czasowe: 28 days
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Maximum Tolerated Dose refers to the highest dose of TG02 administered that will produce the desired effect without unacceptable toxicity.
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28 days
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Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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Safety
Ramy czasowe: 28 days
|
Safety data will include vital signs, ECGs, PE findings, clinical laboratory parameters, ECOG PS, AEs/SAEs and concomitant medications.
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28 days
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Pharmacokinetics of TG02
Ramy czasowe: 28 days
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Plasma will be analyzed to determine TG02 concentration.
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28 days
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Clinical Benefit Response
Ramy czasowe: 28 days
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Clinical Benefit Response is defined as the sum of all response categories for Overall Response Rate (ORR is defined as the sum of patients with sCR, CR, VGPR and PR) plus minimal response (MR).
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28 days
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Overall Response Rate
Ramy czasowe: 28 days
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Overall Response Rate is defined as the sum of patients with sCR, CR, VGPR and PR.
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28 days
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Progression-Free Survival
Ramy czasowe: 28 days
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Progression-Free Survival is the time to disease progression or death, which is measured from the date of first study drug administration until the first date that recurrent or progressive disease is objectively documented or the date of death.
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28 days
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Overall Survival
Ramy czasowe: 28 days
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Overall Survival is time to death, which is measured from the date of first study drug administration until the date of death.
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28 days
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Duration of Response
Ramy czasowe: 28 days
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Duration of Response is the duration from first observation of response to the first documentation of disease progression, with deaths from causes other than disease progression censored.
For the purposes of the calculation of the DOR, the date at which the response status was first observed rather than the date of confirmation is used as the start date.
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28 days
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Pharmacodynamics
Ramy czasowe: 28 days
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Pharmacodynamic sampling may include whole blood and bone marrow at baseline and post-treatment for pathway determination if available.
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28 days
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Współpracownicy i badacze
Sponsor
Śledczy
- Dyrektor Studium: T Parrott, Tragara Pharmaceuticals
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów
Zakończenie podstawowe (Rzeczywisty)
Ukończenie studiów (Rzeczywisty)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Oszacować)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Oszacować)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Dodatkowe istotne warunki MeSH
- Procesy patologiczne
- Choroby układu krążenia
- Choroby naczyniowe
- Choroby układu odpornościowego
- Nowotwory według typu histologicznego
- Nowotwory
- Zaburzenia limfoproliferacyjne
- Zaburzenia immunoproliferacyjne
- Nowotwory według lokalizacji
- Choroby szpiku kostnego
- Choroby hematologiczne
- Zaburzenia krwotoczne
- Zaburzenia mieloproliferacyjne
- Zaburzenia hemostatyczne
- Paraproteinemie
- Zaburzenia białek krwi
- Procesy Nowotworowe
- Nowotwory, komórki plazmatyczne
- Białaczka
- Transformacja komórkowa, nowotworowa
- Rakotwórczość
- Białaczka, mieloidalna
- Białaczka, szpikowa, przewlekła, BCR-ABL dodatnia
- Nowotwory hematologiczne
- Szpiczak mnogi
- Kryzys wybuchowy
- Fizjologiczne skutki leków
- Agenci autonomiczni
- Agenty obwodowego układu nerwowego
- Środki przeciwzapalne
- Środki przeciwnowotworowe
- Leki przeciwwymiotne
- Środki żołądkowo-jelitowe
- Glikokortykosteroidy
- Hormony
- Hormony, substytuty hormonów i antagoniści hormonów
- Środki przeciwnowotworowe, hormonalne
- Deksametazon
Inne numery identyfikacyjne badania
- TG02-101
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