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Biobank of Acute Leukemia to study disease biology

Biorepository of Acute Leukemia for Investigating the Biology of High Risk, Relapsed and Refractory Leukemias - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/04/085648
Enrollment
680
Registered
2025-04-25
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: C950- Acute leukemia of unspecified celltype

Interventions

Intervention1: NIL: NIL Control Intervention1: NIL: NIL

Sponsors

Indian Council of Medical Research (ICMR)
Lead Sponsor
Jawaharlal Institute of Postgraduate Medical Education Research JIPMER
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Inclusion criteria a) All newly diagnosed patients with acute leukemia who are registered in the Department of Medical Oncology b) Either a diagnosis of ALL, AML, or APML c) Patients who are treatment naive d) All age groups and gender

Exclusion criteria

Exclusion criteria: Exclusion criteria a) patients who refuse to give consent b) pregnant women with acute leukemia

Design outcomes

Primary

MeasureTime frame
1. Establish a biorepository for acute leukemia with well-annotated clinical data.Timepoint: 1. Baseline at diagnosis[T1] 2. At remission (21-28 days) [T2] 3. At treatment completion (if feasible)[T3] 4. At relapse (where applicable)[T4]

Secondary

MeasureTime frame
1. Augment in-house laboratory capacity in leukemia-specific advanced investigations 2. Support the conduct of local need-based translational studies for high-risk and relapsed/refractory acute leukemia in the focused areas defined in the CAR project. 3. Provide a platform to conduct future studies investigating different biological and clinical aspects of this rare but potentially curable malignancy and eventually become a resource for clinicians, and basic scientists.Timepoint: 1. Baseline at diagnosis[T1] 2. At remission (21-28 days) [T2] 3. At treatment completion (if feasible)[T3] 4. At relapse (where applicable)[T4]

Countries

India

Contacts

Public ContactDr Smita Kayal

Jawaharlal Institute of Postgraduate Medical Education & Research

kayalsmita@gmail.com7598118439

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026