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Non-Hodgkin Lymphoma

Oncology 1 original drugs
1
Novel Drugs
6
Reformulations
1,604
Active Trials
5
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
Ibrutinib
Johnson & Johnson
Estimated · fresh NCT01804686
Q1 2027
zanubrutinib
BeOne Medicines
Estimated · aging NCT04002297
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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 12 mechanisms across 48 industry trials with a known mechanism of action.

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Kinase Inhibitor
20 trials 5 active 7 sponsors
DNA
5 trials 3 active 3 sponsors
CD20-directed Cytolytic Antibody
4 trials 1 active 2 sponsors
Thalidomide Analog
4 trials 2 sponsors
Programmed Death Receptor-1 Blocking Antibody
4 trials 2 sponsors
PI3K-delta/PI3K-gamma
3 trials 2 sponsors
CD30-directed Immunoconjugate
2 trials 1 sponsor
CD19/CD3
2 trials 1 sponsor
AKT1/AKT2/AKT3
1 trials 1 sponsor
Proteasome Inhibitor
1 trials 1 sponsor
BCL-2 Inhibitor
1 trials 1 sponsor
Nuclear Export Inhibitor
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

397 industry-sponsored trials across 203 sponsors

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Novel Drugs by Company (New molecular entities)

Reformulations (6 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 (4 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