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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03216070
Other study ID # HE17 00004
Secondary ID
Status Recruiting
Phase Phase 4
First received July 10, 2017
Last updated July 10, 2017
Start date April 1, 2016
Est. completion date October 1, 2018

Study information

Verified date July 2017
Source Hospital Universitario Dr. Jose E. Gonzalez
Contact David Gomez, MD
Phone 52 81 8348-8510
Email dr_gomez@infosel.net.mx
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Our goal is to demonstrate that 50mg of dasatinib is as effective as the full dose to induce molecular response as first line therapy in CML.


Description:

We will give 50mg of dasatinib daily since the diagnosis for up to 6 months, for the first 2-4 weeks we will evaluate hematic biometry to registry hematic response, at months 3 and 6 a BCR/ABL PCR will be taken to evaluate molecular response.


Recruitment information / eligibility

Status Recruiting
Enrollment 12
Est. completion date October 1, 2018
Est. primary completion date October 1, 2018
Accepts healthy volunteers No
Gender Female
Age group 16 Years and older
Eligibility Inclusion Criteria:

- Diagnosis of BCR-ABL positive CML in early chronic phase CML. Except for hydroxyurea, patients must have received no or minimal prior therapy, defined as <2 weeks (14 days) of prior FDA approved TKI.

- ECOG performance of 0-2

- Adequate end organ function, defined as the following: total bilirubin <1.5x ULN, SGPT <2.5x ULN, creatinine <1.5x ULN.

- Patients must sign an informed consent indicating they are aware of the investigational nature of this study.

Exclusion Criteria:

- NYHA cardiac class 3-4 heart disease or previous pleural effusion.

- Pregnancy and lactation

- Patients with active, uncontrolled psychiatric disorders

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Dasatinib 50 MG
50mg of dasatinib orally daily

Locations

Country Name City State
Mexico Hopsital Universitario Dr. Jose E. Gonzalez, Centro Universitario contra el Cancer Monterrey Nuevo Leon

Sponsors (1)

Lead Sponsor Collaborator
Hospital Universitario Dr. Jose E. Gonzalez

Country where clinical trial is conducted

Mexico, 

References & Publications (5)

Kantarjian H, Shah NP, Hochhaus A, Cortes J, Shah S, Ayala M, Moiraghi B, Shen Z, Mayer J, Pasquini R, Nakamae H, Huguet F, Boqué C, Chuah C, Bleickardt E, Bradley-Garelik MB, Zhu C, Szatrowski T, Shapiro D, Baccarani M. Dasatinib versus imatinib in newly diagnosed chronic-phase chronic myeloid leukemia. N Engl J Med. 2010 Jun 17;362(24):2260-70. doi: 10.1056/NEJMoa1002315. Epub 2010 Jun 5. — View Citation

Keskin D, Sadri S, Eskazan AE. Dasatinib for the treatment of chronic myeloid leukemia: patient selection and special considerations. Drug Des Devel Ther. 2016 Oct 13;10:3355-3361. eCollection 2016. Review. — View Citation

Shah NP, Kantarjian HM, Kim DW, Réa D, Dorlhiac-Llacer PE, Milone JH, Vela-Ojeda J, Silver RT, Khoury HJ, Charbonnier A, Khoroshko N, Paquette RL, Deininger M, Collins RH, Otero I, Hughes T, Bleickardt E, Strauss L, Francis S, Hochhaus A. Intermittent target inhibition with dasatinib 100 mg once daily preserves efficacy and improves tolerability in imatinib-resistant and -intolerant chronic-phase chronic myeloid leukemia. J Clin Oncol. 2008 Jul 1;26(19):3204-12. doi: 10.1200/JCO.2007.14.9260. Epub 2008 Jun 9. — View Citation

Stein B, Smith BD. Treatment options for patients with chronic myeloid leukemia who are resistant to or unable to tolerate imatinib. Clin Ther. 2010 May;32(5):804-20. doi: 10.1016/j.clinthera.2010.05.003. Review. — View Citation

Tokarski JS, Newitt JA, Chang CY, Cheng JD, Wittekind M, Kiefer SE, Kish K, Lee FY, Borzillerri R, Lombardo LJ, Xie D, Zhang Y, Klei HE. The structure of Dasatinib (BMS-354825) bound to activated ABL kinase domain elucidates its inhibitory activity against imatinib-resistant ABL mutants. Cancer Res. 2006 Jun 1;66(11):5790-7. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Molecular Response at 6 months Molecular Response define as BCR/ABL <1% 6 months
Secondary Early Molecular Response at 3 and 6 months Early Molecular Response define as <10% 3 and 6 months
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