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Chronic Lymphocytic Leukemia

Oncology 7 original drugs
7
Novel Drugs
9
Reformulations
0
Active Trials
6
Drug Targets

Phase 3 Readouts Pro

12 active Phase 3 trials with confidence-graded completion dates.

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Q2 2026
Xembify
Grifols Therapeutics LLC
Estimated · fresh NCT05645107
Q4 2026
Pirtobrutinib
Loxo Oncology, Inc.
Estimated · fresh NCT04965493
Q4 2026
Ibrutinib
Johnson & Johnson
Estimated · fresh NCT01804686
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Anchored on CT.gov primary completion date. Topline announcements typically precede this by 3–9 months. Confidence labels combine date type (ACTUAL/ESTIMATED) with last-update freshness.

Treatments by Mechanism

Top 9 mechanisms across 64 industry trials with a known mechanism of action.

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Kinase Inhibitor
34 trials 10 active 7 sponsors
BCL-2 Inhibitor
10 trials 5 active 3 sponsors
CD20-directed Cytolytic Antibody
9 trials 1 active 7 sponsors
Thalidomide Analog
3 trials 1 sponsor
PI3K-delta/PI3K-gamma
3 trials 2 sponsors
Alkylating Drug
2 trials 2 sponsors
CD52-directed Cytolytic Antibody
1 trials 1 sponsor
Hematopoietic Stem Cell Mobilizer
1 trials 1 sponsor
ABL kinase/BCR-ABL/EPHA2/FYN/LCK/PDGFRβ/SRC/YES/c-KIT
1 trials 1 sponsor

MoA derived from FDA pharmClassEpc when intervention matches an approved drug. Codenamed clinical-stage assets without an approved counterpart show "—" and aren't grouped here — they're still in the phase tables below.

Clinical Pipeline by Phase

287 industry-sponsored trials across 113 sponsors

Precision Medicine Biomarkers

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Biomarkers used for patient selection in Chronic Lymphocytic Leukemia

Reformulations (9 drugs) Click to expand

Reformulations are FDA-approved versions of existing molecules in new dosage forms (e.g., oral solution vs tablet, extended-release vs immediate-release). They require a new NDA but use an already-proven active ingredient.

Generic Drugs (1 ANDA approved) Click to expand

Generic drugs contain the same active ingredient as the brand-name drug and are approved via ANDA (Abbreviated New Drug Application).

Related Indications

Other Oncology indications

Drug Categories:

  • Novel Drugs: NDA Type 1/2 (new molecular entity) or original BLA
  • Reformulations: NDA Type 3/5 (new dosage form of existing molecule)
  • Biosimilars: BLA-approved biologics highly similar to reference products
  • Generics: ANDA-approved copies of small molecule drugs

View data sources and methodology