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Phase 1 Study of TG02 Citrate in Patients With Advanced Hematological Malignancies (TG02-101)

2016年5月5日 更新者:Tragara Pharmaceuticals, Inc.

Phase 1 Dose-Escalation and Pharmacokinetic Study of TG02 Citrate in Patients With Advanced Hematological Malignancies

This is a multicenter, open-label, dose escalation Phase 1 study.

調査の概要

詳細な説明

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.

研究の種類

介入

入学 (予想される)

120

段階

  • フェーズ 1

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

    • Colorado
      • Denver、Colorado、アメリカ、80218
        • RMCC
    • Georgia
      • Atlanta、Georgia、アメリカ、30322
        • EMORY
    • Illinois
      • Chicago、Illinois、アメリカ、60612
        • Rush
    • Indiana
      • Indianapolis、Indiana、アメリカ、46202
        • IU
    • New Jersey
      • Hackensack、New Jersey、アメリカ、07601
        • HUMC
    • New York
      • New York City、New York、アメリカ、10021
        • Cornell
    • Ohio
      • Columbus、Ohio、アメリカ、43210
        • OSU
    • Tennessee
      • Nashville、Tennessee、アメリカ、37203
        • SCRI
    • Texas
      • Houston、Texas、アメリカ、77030
        • MDACC

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年歳以上 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

説明

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

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:非ランダム化
  • 介入モデル:単一グループの割り当て
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的:TG02 in AL
Single agent TG02 citrate in acute leukemia patients
TG02 citrate capsules given orally.
他の名前:
  • 他の名前はありません。
実験的:TG02 in MM
Single Agent TG02 citrate in multiple myeloma patients
TG02 citrate capsules given orally.
他の名前:
  • 他の名前はありません。
実験的:TG02 + CFZ in MM
TG02 in combination with carfilzomib and dexamethasone in multiple myeloma patients
TG02 citrate capsules given orally.
他の名前:
  • 他の名前はありません。
Carfilzomib per PI
他の名前:
  • キプロリス
実験的:TG02 + CFZ + DEX in CFZ refractory MM
TG02 in combination with carfilzomib and dexamethasone in carfilzomib refractory multiple myeloma patients
TG02 citrate capsules given orally.
他の名前:
  • 他の名前はありません。
Carfilzomib per PI
他の名前:
  • キプロリス
Dexamethasone (Oral or IV)
他の名前:
  • Ozurdex, Maxidex, Decadron, Baycadron

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Maximum Tolerated Dose
時間枠:28 days
Maximum Tolerated Dose refers to the highest dose of TG02 administered that will produce the desired effect without unacceptable toxicity.
28 days

二次結果の測定

結果測定
メジャーの説明
時間枠
Safety
時間枠:28 days
Safety data will include vital signs, ECGs, PE findings, clinical laboratory parameters, ECOG PS, AEs/SAEs and concomitant medications.
28 days
Pharmacokinetics of TG02
時間枠:28 days
Plasma will be analyzed to determine TG02 concentration.
28 days
Clinical Benefit Response
時間枠:28 days
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).
28 days
Overall Response Rate
時間枠:28 days
Overall Response Rate is defined as the sum of patients with sCR, CR, VGPR and PR.
28 days
Progression-Free Survival
時間枠:28 days
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.
28 days
Overall Survival
時間枠:28 days
Overall Survival is time to death, which is measured from the date of first study drug administration until the date of death.
28 days
Duration of Response
時間枠:28 days
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.
28 days
Pharmacodynamics
時間枠:28 days
Pharmacodynamic sampling may include whole blood and bone marrow at baseline and post-treatment for pathway determination if available.
28 days

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

捜査官

  • スタディディレクター:T Parrott、Tragara Pharmaceuticals

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始

2010年8月1日

一次修了 (実際)

2016年3月1日

研究の完了 (実際)

2016年4月1日

試験登録日

最初に提出

2010年9月14日

QC基準を満たした最初の提出物

2010年9月15日

最初の投稿 (見積もり)

2010年9月17日

学習記録の更新

投稿された最後の更新 (見積もり)

2016年5月6日

QC基準を満たした最後の更新が送信されました

2016年5月5日

最終確認日

2016年5月1日

詳しくは

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

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