- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT07471841
Olutasidenib in Pazienti con AML Recidivante Mutata per IDH1 che Hanno Precedentemente Ricevuto Venetoclax
Studio pilota di fase 2 a braccio singolo di Olutasidenib in pazienti con AML mutata IDH1 recidivata che hanno precedentemente ricevuto Venetoclax
This is a prospective, single-arm phase 2 pilot study to assess the response rate of IDH1 mutated relapsed/refractory acute myeloid leukemia (AML) patients who receive olutasidenib after progressing on venetoclax based regimens. Each cycle will last for 28 days. Patients will receive olutasidenib 150 mg orally twice daily Day 1 through Day 28. After 3 cycles of olutasidenib, azacitidine 75 mg/m2 given on Day 1 through Day 7 may be added at the discretion of the treating investigator if the patient has not achieved a complete remission. Subjects with at least a PR after 6 cycles of treatment will continue treatment as previously described. Subjects without at least a partial response (PR) after 6 cycles of treatment will move to long term follow up.
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Tipo di studio
Iscrizione (Stimato)
Fase
- Fase 2
Contatti e Sedi
Contatto studio
- Nome: Ahran Lee
- Numero di telefono: 14 317-634-5842
- Email: alee@hoosiercancer.org
Backup dei contatti dello studio
- Nome: Timothy Pardee
- Numero di telefono: MD, PhD
- Email: Timothy.Pardee@wfusm.edu
Luoghi di studio
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North Carolina
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Winston-Salem, North Carolina, Stati Uniti, 27157
- Reclutamento
- Atrium Health Wake Forest Baptist Medical Center
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Investigatore principale:
- Timothy Pardee, MD, PhD
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Contatto:
- Elizabeth Parke
- Numero di telefono: 980-442-2000
- Email: Elizabeth.Parke@Advocatehealth.org
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria:
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Written informed consent and HIPAA authorization for release of personal health information prior to registration. NOTE: HIPAA authorization may be included in the informed consent or obtained separately.
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Age ≥ 18 years at the time of consent.
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ECOG Performance Status of ≤ 2 within 28 days prior to registration.
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Must have histologically or cytologically documented relapsed and/or refractory Acute Myeloid Leukemia (Refractory is defined as failure to achieve a CR after induction chemotherapy or a minimum of two cycles of HMA plus venetoclax)
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Acute Myeloid Leukemia with a documented IDH1 mutation.
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No more than 2 lines of prior therapy. NOTE: One line of therapy must have contained venetoclax.
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Persisting, non-hematologic and non-infectious toxicities from prior treatment must be Grade ≤ 2. NOTE: Documentation of these criteria is required at screening.
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Demonstrate adequate organ function as defined in the table below. All screening labs to be obtained within 14 days prior to registration.
- Renal
- Calculated creatinine clearance (Cockcroft-Gault formula will be used to calculate creatinine clearance) ≥ 30 mL/min
- Hepatic
- Total bilirubin2 ≤ 2× upper limit of normal (ULN); ≤ 3 times ULN in patients with Gilbert Syndrome
- Aspartate aminotransferase (AST) ≤ 5 × ULN
- Alanine aminotransferase (ALT) ≤ 5× ULN
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Participants of childbearing potential must have a negative serum pregnancy test within 7 days prior to initiation of treatment.
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Participants of childbearing potential who are having penile-vaginal intercourse with a person able to father a child must be willing to abstain from penile-vaginal intercourse or must use an effective method(s) of contraception. A participant able to father a child who is having penile-vaginal intercourse with a person of childbearing potential must be willing to abstain from penile-vaginal intercourse or use an effective method(s) of contraception.
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Subjects with known HIV infection may be eligible if they are on effective anti-retroviral therapy with undetectable viral load within 6 months prior to registration. Testing is not required at screening.
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Subjects with known chronic hepatitis B virus (HBV) infection may be eligible if they have an undetectable HBV viral load on suppressive therapy, if indicated. Subjects with a history of hepatitis C virus (HCV) infection may be eligible if they have been treated and cured. Subjects with an HCV infection who are currently on treatment must have an undetectable HCV viral load to be eligible for this trial. Testing is not required at screening.
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As determined by the investigator or protocol designee, ability of the subject to understand and comply with study procedures for the entire length of the study.
Exclusion Criteria:
- Previous exposure to ivosidenib or any IDH1 inhibitor.
- Active infection requiring IV systemic therapy. NOTE: Subjects receiving prophylactic antibiotics (e.g., to prevent a urinary tract infection or chronic obstructive pulmonary disease exacerbation) are eligible for the study.
- Known CNS involvement with AML.
- Previous allogeneic stem cell transplant within 60 days prior to registration.
- Treatment with any investigational drug within 21 days or 2 half-life's prior to registration.
- History of severe allergic anaphylactic reactions to olutasidenib or any of their excipients.
- Pregnant or breastfeeding. NOTE: breast milk cannot be stored for future use while the subject is being treated on study.
- Prior or concurrent malignancy whose natural history or treatment has the potential to interfere with the safety or efficacy assessment of the investigational regimen, per treating physician discretion.
- Concomitant use of known strong (e.g. phenobarbital, enzalutamide, phenytoin, rifampicin, rifabutin, rifapentine, carbamazepine, nevirapine and St John's Wort) or moderate CYP3A inducers (e.g. bosentan, efavirenz, modafinil). The required washout period prior to starting olutasidenib is 2 weeks or 5 half-lives (whichever is longer) prior to initiation of treatment.
- Concomitant use of known sensitive CYP3A substrates (e.g. Midazolam, simvastatin, fluticasone, budesonide). The required washout period prior to starting olutasidenib is 2 weeks or 5 half-lives (whichever is longer) prior to initiation of treatment.
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: N / A
- Modello interventistico: Assegnazione di gruppo singolo
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
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Sperimentale: Olutasidenib and Azacitidine
Each cycle will last for 28 days. Patients will receive olutasidenib 150 mg orally twice daily Day 1 through Day 28. After 3 cycles of olutasidenib, azacitidine 75 mg/m2 given on Day 1 through Day 7 may be added at the discretion of the treating investigator if the patient has not achieved a complete remission or for whom loss of response is suspected. Subjects with at least a PR after 6 cycles of treatment will continue treatment.. Subjects without at least a PR after 6 cycles of treatment will move to long term follow up. |
Olutasidenib 150 mg orally twice a day Azacitidine 75 mg/m2 subcutaneously or IV (over 10-40 minutes) |
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Composite complete remission rate
Lasso di tempo: 2 years
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Composite complete remission (CRc) rate is defined as patients that meet the criteria for CR + CRh + CRi per the modified European LeukemiaNet (mELN) 2022.
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2 years
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Overall response rate (ORR)
Lasso di tempo: 2 years
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ORR is defined as the proportion of patients achieving CR + CRh + CRi + Partial Remission (PR) + morphologic leukemia-free state [MLFS] per ELN 2022. PR is defined as all hematologic criteria of CR; decrease of bone marrow blast percentage to 5% to 25%; and decrease of pretreatment bone marrow blast percentage by at least 50%. MLFS is defined as bone marrow blasts < 5%, absence of circulating blasts, and no hematologic recovery. |
2 years
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Overall survival
Lasso di tempo: 2 years
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OS is defined as the time from registration to death from any cause or last known follow-up. |
2 years
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Duration of response (DoR)
Lasso di tempo: 2 years
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DoR is defined as the time between the first achieved response (CR, CRh, CRi, PR, MLFS) and the earliest evidence of relapse (blasts ≥ 5%) per ELN 2022 or death or date of last follow up. |
2 years
|
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Time to hematologic improvement (hemoglobin)
Lasso di tempo: 2 years
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Improvement of Hgb is defined as the time it takes for an individual's hemoglobin level to increase by ≥ 1g/dL from Cycle 1 Day 1 without transfusion |
2 years
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Time to hematologic improvement (platelet count)
Lasso di tempo: 2 years
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Improvement of PLT is defined as the time it takes for an individual's platelet count to increase by ≥ 50 x 10^9/L from Cycle 1 Day 1 without transfusion |
2 years
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Time to hematologic improvement (neutrophil count)
Lasso di tempo: 2 years
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Improvement of ANC is defined as the time it takes for an individual's neutrophil count to increase to ≥ 1,500 cells/µL for 3 days. |
2 years
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Rate of transfusion independence
Lasso di tempo: 2 years
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The rate of transfusion independence is defined as the absence of red blood cell (RBC) transfusions for ≥ 8 weeks following the start of treatment |
2 years
|
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Rate of allogeneic transplant
Lasso di tempo: 2 years
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The rate of allogeneic transplant is defined as the proportion of patients who undergo allogeneic transplant following response to olutasidenib. |
2 years
|
Collaboratori e investigatori
Sponsor
Investigatori
- Investigatore principale: Timothy Pardee, MD, PhD, Atrium Health Wake Forest Baptist
Studiare le date dei record
Studia le date principali
Inizio studio (Stimato)
Completamento primario (Stimato)
Completamento dello studio (Stimato)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
- Neoplasie
- Neoplasie per tipo istologico
- Malattie ematologiche
- Leucemia, mieloide
- Leucemia
- Malattie emiche e linfatiche
- Leucemia, mieloide, acuta
- Prodotti chimici organici
- Composti eterociclici, 1-anello
- Composti eterociclici
- Acidi nucleici, nucleotidi e nucleosidi
- Citidina
- Nucleosidi di pirimidina
- Pirimidine
- Composti aza
- Nucleosidi
- Ribonucleosidi
- Azacitidina
- olutasidenib
Altri numeri di identificazione dello studio
- HCRN-AML24-687
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
prodotto fabbricato ed esportato dagli Stati Uniti
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