Trial Radar
Sign in

NCT lookup

Pull any trial record directly from ClinicalTrials.gov.

Study of Acalabrutinib Versus Chlorambucil Plus Rituximab in Adult Subjects With Previously Untreated Chronic Lymphocytic Leukemia
Study of Acalabrutinib Versus Chlorambucil Plus Rituximab in Adult Subjects With Previously Untreated Chronic Lymphocytic Leukemia

NCT04075292

Active Not RecruitingPhase 3

Sponsor: AstraZeneca

Conditions: Untreated Chronic Lymphocytic Leukemia

Interventions: Acalabrutinib, Rituximab, Chlorambucil

Countries: China, Philippines, Taiwan, Thailand, Vietnam

This is a randomized, multicenter, open-label, Phase 3 study to evaluate the efficacy and safety of Acalabrutinib versus Chlorambucil plus Rituximab in subjects with Previously Untreated Chronic Lymphocytic Leukemia.

Eligibility overview

Sex: ALL

Age: 18 Years to 130 Years

Healthy volunteers: No

Study type: INTERVENTIONAL

Eligibility criteria
Inclusion Criteria:

* Men and women: (a) ≥65 years of age OR (b) \>18 and \<65 years of age, provided that they meet at least one of the following criteria: (i) Creatinine clearance 30 to 69 mL/min using the Cockcroft-Gault equation (iwCLL guidelines) (ii) A score higher than 6 on the Cumulative Illness Rating Score-Geriatric (CIRS G)
* ECOG performance status of 0, 1, or 2
* Diagnosis of CLL that meets published diagnostic criteria (Hallek 2018)
* Active disease per IWCLL 2018 criteria that requires treatment
* Adequate bone marrow function
* Adequate renal and hepatic function

Exclusion Criteria:

* Known detected del(17p) or TP53 mutation
* Transformation of CLL to aggressive non-Hodgkin lymphoma (NHL) (eg, Richter's transformation, PLL, or diffuse large B cell lymphoma \[DLBCL\]), or central nervous system (CNS) involvement by leukemia
* History of prior malignancy except for the following: (a) Curatively treated basal cell carcinoma or squamous cell carcinoma of the skin or carcinoma in situ of the cervix at any time prior to study (b) Other cancers not specified above which have been curatively treated by surgery and/or radiation therapy from which subject is disease-free for ≥3 years without further treatment
* Significant cardiovascular disease
* Known history of infection with human immunodeficiency virus (HIV)
* Serologic status reflecting active hepatitis B or C infection
* Any active systemic infection (eg, bacterial, viral, or fungal infection) requiring systemic treatment
* History of stroke or intracranial hemorrhage within 6 months before first dose of study drug
* Major surgical procedure within 30 days of first dose of study drug
* Any prior CLL-specific therapies
* Corticosteroid use \>20 mg within 1 week before first dose of study drug, except as indicated for other medical conditions
* Requires or receiving anticoagulation with warfarin or equivalent vitamin K antagonists
* For women only: breastfeeding or pregnant
Locations (46)
  • Beijing, China
  • Changchun, China
  • Changsha, China
  • Changzhou, China
  • Guangzhou, China
  • Guangzhou, China
  • Guiyang, China
  • Hangzhou, China
  • Hefei, China
  • Hefei, China
  • Nanchang, China
  • Nanjing, China
  • Qingdao, China
  • Shanghai, China
  • Shanghai, China
  • Shanghai, China
  • Shenyang, China
  • Shijiazhuang, China
  • Suzhou, China
  • Taiyuan, China
  • Tianjin, China
  • Xuzhou, China
  • Zhengzhou, China
  • Zhengzhou, China
  • Baguio City, Philippines
  • Cebu, Philippines
  • Davao City, Philippines
  • Makati, Philippines
  • Manila, Philippines
  • Quezon City, Philippines
  • + 16 more on CT.gov