- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica 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
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
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.
Tipo di studio
Iscrizione (Anticipato)
Fase
- Fase 1
Contatti e Sedi
Luoghi di studio
-
-
Colorado
-
Denver, Colorado, Stati Uniti, 80218
- RMCC
-
-
Georgia
-
Atlanta, Georgia, Stati Uniti, 30322
- EMORY
-
-
Illinois
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Chicago, Illinois, Stati Uniti, 60612
- Rush
-
-
Indiana
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Indianapolis, Indiana, Stati Uniti, 46202
- IU
-
-
New Jersey
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Hackensack, New Jersey, Stati Uniti, 07601
- HUMC
-
-
New York
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New York City, New York, Stati Uniti, 10021
- Cornell
-
-
Ohio
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Columbus, Ohio, Stati Uniti, 43210
- OSU
-
-
Tennessee
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Nashville, Tennessee, Stati Uniti, 37203
- SCRI
-
-
Texas
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Houston, Texas, Stati Uniti, 77030
- MDACC
-
-
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
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
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Non randomizzato
- Modello interventistico: Assegnazione di gruppo singolo
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Sperimentale: TG02 in AL
Single agent TG02 citrate in acute leukemia patients
|
TG02 citrate capsules given orally.
Altri nomi:
|
|
Sperimentale: TG02 in MM
Single Agent TG02 citrate in multiple myeloma patients
|
TG02 citrate capsules given orally.
Altri nomi:
|
|
Sperimentale: TG02 + CFZ in MM
TG02 in combination with carfilzomib and dexamethasone in multiple myeloma patients
|
TG02 citrate capsules given orally.
Altri nomi:
Carfilzomib per PI
Altri nomi:
|
|
Sperimentale: 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.
Altri nomi:
Carfilzomib per PI
Altri nomi:
Dexamethasone (Oral or IV)
Altri nomi:
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Maximum Tolerated Dose
Lasso di tempo: 28 days
|
Maximum Tolerated Dose refers to the highest dose of TG02 administered that will produce the desired effect without unacceptable toxicity.
|
28 days
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Safety
Lasso di tempo: 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
Lasso di tempo: 28 days
|
Plasma will be analyzed to determine TG02 concentration.
|
28 days
|
|
Clinical Benefit Response
Lasso di tempo: 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
Lasso di tempo: 28 days
|
Overall Response Rate is defined as the sum of patients with sCR, CR, VGPR and PR.
|
28 days
|
|
Progression-Free Survival
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 28 days
|
Pharmacodynamic sampling may include whole blood and bone marrow at baseline and post-treatment for pathway determination if available.
|
28 days
|
Collaboratori e investigatori
Sponsor
Investigatori
- Direttore dello studio: T Parrott, Tragara Pharmaceuticals
Studiare le date dei record
Studia le date principali
Inizio studio
Completamento primario (Effettivo)
Completamento dello studio (Effettivo)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Stima)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Stima)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
- Processi patologici
- Malattia cardiovascolare
- Malattie vascolari
- Malattie del sistema immunitario
- Neoplasie per tipo istologico
- Neoplasie
- Malattie linfoproliferative
- Disturbi immunoproliferativi
- Neoplasie per sede
- Malattie del midollo osseo
- Malattie ematologiche
- Disturbi emorragici
- Malattie mieloproliferative
- Disturbi emostatici
- Paraproteinemie
- Disturbi delle proteine del sangue
- Processi neoplastici
- Neoplasie, plasmacellule
- Leucemia
- Trasformazione cellulare, neoplastica
- Cancerogenesi
- Leucemia, mieloide
- Leucemia, Mielogena, Cronica, BCR-ABL Positivo
- Neoplasie ematologiche
- Mieloma multiplo
- Crisi esplosiva
- Effetti fisiologici delle droghe
- Agenti autonomi
- Agenti del sistema nervoso periferico
- Agenti antinfiammatori
- Agenti antineoplastici
- Antiemetici
- Agenti gastrointestinali
- Glucocorticoidi
- Ormoni
- Ormoni, sostituti ormonali e antagonisti ormonali
- Agenti antineoplastici, ormonali
- Desametasone
Altri numeri di identificazione dello studio
- TG02-101
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .