Duvelisib
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Also known as INK-1147INK-1197IPI-145DUVELISIB (IPI-145, INK1197)DuvelisibCopiktraDuvelisib (IPI-145INK1197)
Summary
Duvelisib (CHEMBL3039502) is an approved small molecule (ATC L01EM04) targeting PIK3CA, PIK3CB, and PIK3CD; indicated across 20 conditions including neoplasm and b-cell chronic lymphocytic leukemia.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Small molecule
- ATC class: L01EM04
- Targets: 4 (PIK3CA, PIK3CB, PIK3CD…)
- Indications: 20 conditions
- Clinical trials: 55
- Chemistry: 416.9 Da · C22H17ClN6O
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL3039502 |
| Name | Duvelisib |
| Type | Small molecule |
| Max phase | 4 |
| FDA approved | yes |
| PubChem CID | 50905713 |
| ATC | L01EM04 |
| Molecular formula | C22H17ClN6O |
| Molecular weight | 416.9 |
| InChIKey | SJVQHLPISAIATJ-ZDUSSCGKSA-N |
SMILES: C[C@@H](C1=CC2=C(C(=CC=C2)Cl)C(=O)N1C3=CC=CC=C3)NC4=NC=NC5=C4NC=N5
IUPAC name: 8-chloro-2-phenyl-3-[(1S)-1-(7H-purin-6-ylamino)ethyl]isoquinolin-1-one
Also known as: Duvelisib, INK-1147, INK-1197, IPI-145, DUVELISIB, DUVELISIB (IPI-145, INK1197), Duvelisib; Copiktra, Duvelisib (IPI-145; INK1197), duvelisib
Parent form; salt/anhydrous children: CHEMBL5315125
Patent coverage: 2,039 distinct patent families (5,332 SureChEMBL compound mentions), from 8 matched compound structure(s). One matched structure accounts for 4,787 (90%) of the total. Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.
Targets
Targets
Primary targets (GtoPdb curated mechanism): the Cancer dependency column is the DepMap CRISPR fitness signal (% of screened cell lines dependent on the target).
| Gene | Target | Action | pAffinity | Cancer dependency | UniProt |
|---|---|---|---|---|---|
| PIK3CA | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Inhibition | 5.8 | 42.7% | P42336 |
| PIK3CB | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta | Inhibition | 7.07 | 5% | P42338 |
| PIK3CD | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | Inhibition | 8.6 | 6% | O00329 |
| PIK3CG | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma | Inhibition | 7.57 | 0.7% | P48736 |
Broader ChEMBL bioactivity targets: 13 (assay-derived). Sample: Thromboxane A2 receptor, PI3-kinase p110-alpha/p85-alpha, PI3-kinase p110-delta/p85-alpha, Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform, 5-hydroxytryptamine receptor 2A, cGMP-inhibited 3’,5’-cyclic phosphodiesterase 3A, PI3K p110 beta/p85 alpha, Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform, Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform, Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform, Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform/gamma isoform, Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform, Bile salt export pump.
Bioactivity
ChEMBL activities: 41 potent at pChembl ≥ 5 of 45 total. Top 100 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| PIK3CD | 9.62 | IC50 | 0.24 | nM | CHEMBL_ACT_25556643 |
| PIK3CD | 9 | IC50 | 1 | nM | CHEMBL_ACT_19041450 |
| PIK3CD | 9 | IC50 | 1 | nM | CHEMBL_ACT_19041569 |
| PIK3CG | 8.7 | IC50 | 2 | nM | CHEMBL_ACT_19041427 |
| PIK3CD | 8.64 | IC50 | 2.3 | nM | CHEMBL_ACT_18769660 |
| PIK3CG | 8.6 | IC50 | 2.5 | nM | CHEMBL_ACT_18952540 |
| PIK3CD | 8.6 | IC50 | 2.5 | nM | CHEMBL_ACT_19036925 |
| PIK3CD | 8.6 | IC50 | 2.5 | nM | CHEMBL_ACT_24766729 |
| PIK3CD | 8.6 | IC50 | 2.5 | nM | CHEMBL_ACT_24862057 |
| PIK3CD | 8.6 | IC50 | 2.5 | nM | CHEMBL_ACT_26047648 |
| PIK3CD | 8.6 | IC50 | 2.5 | nM | CHEMBL_ACT_26187201 |
| PIK3CG | 8.54 | IC50 | 2.9 | nM | CHEMBL_ACT_16673449 |
| PIK3CD | 8.3 | EC50 | 5 | nM | CHEMBL_ACT_26047686 |
| PIK3R1 | 8.1 | IC50 | 8 | nM | CHEMBL_ACT_19041473 |
| PIK3CG | 7.92 | IC50 | 12 | nM | CHEMBL_ACT_18769663 |
| PIK3CD | 7.85 | IC50 | 14 | nM | CHEMBL_ACT_19041627 |
| PIK3CD | 7.85 | IC50 | 14 | nM | CHEMBL_ACT_26187196 |
| PIK3CG | 7.82 | IC50 | 15 | nM | CHEMBL_ACT_19041631 |
| PIK3CB | 7.68 | EC50 | 21 | nM | CHEMBL_ACT_26047682 |
| PIK3CD | 7.57 | IC50 | 27 | nM | CHEMBL_ACT_18952532 |
| PIK3CG | 7.57 | IC50 | 27 | nM | CHEMBL_ACT_19036926 |
| PIK3CG | 7.57 | IC50 | 27 | nM | CHEMBL_ACT_24766721 |
| PIK3CG | 7.57 | IC50 | 27 | nM | CHEMBL_ACT_25847386 |
| PIK3CG | 7.57 | IC50 | 27 | nM | CHEMBL_ACT_26047647 |
| PIK3CG | 7.57 | IC50 | 27 | nM | CHEMBL_ACT_26187200 |
| PIK3CG | 7.56 | IC50 | 27.4 | nM | CHEMBL_ACT_24862058 |
| PIK3R1 | 7.31 | IC50 | 49 | nM | CHEMBL_ACT_18769657 |
| PIK3CG | 7.3 | IC50 | 50 | nM | CHEMBL_ACT_25556630 |
| Q9JHG7 | 7.29 | IC50 | 51 | nM | CHEMBL_ACT_26187194 |
| Q9JHG7 | 7.14 | EC50 | 72 | nM | CHEMBL_ACT_26047684 |
| PIK3CB | 7.07 | IC50 | 85 | nM | CHEMBL_ACT_18952521 |
| PIK3CB | 7.07 | IC50 | 85 | nM | CHEMBL_ACT_26187199 |
| PIK3CD | 7.02 | IC50 | 96 | nM | CHEMBL_ACT_19474662 |
| PIK3CD | 7 | IC50 | 100 | nM | CHEMBL_ACT_19474663 |
| PIK3CB | 6.52 | IC50 | 301 | nM | CHEMBL_ACT_26187192 |
| PIK3R1 | 6.4 | IC50 | 400 | nM | CHEMBL_ACT_18769654 |
| PIK3CA | 6.15 | EC50 | 711 | nM | CHEMBL_ACT_26047680 |
| PIK3CA | 5.79 | IC50 | 1602 | nM | CHEMBL_ACT_18952525 |
| PIK3CA | 5.79 | IC50 | 1602 | nM | CHEMBL_ACT_26047646 |
| PIK3CA | 5.79 | IC50 | 1602 | nM | CHEMBL_ACT_26187198 |
| PIK3CD | 5.66 | IC50 | 2206 | nM | CHEMBL_ACT_19041633 |
Target pathways
Aggregated over 4 target gene(s): PIK3CA, PIK3CB, PIK3CD, PIK3CG.
Top Reactome pathways
62 total, by targets touching each:
| Pathway | Targets | Genes |
|---|---|---|
| PIP3 activates AKT signaling | 4 | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| Synthesis of PIPs at the plasma membrane | 4 | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| Constitutive Signaling by Aberrant PI3K in Cancer | 4 | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| CD28 dependent PI3K/Akt signaling | 4 | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | 4 | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| Erythropoietin activates Phosphoinositide-3-kinase (PI3K) | 4 | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| Co-stimulation by ICOS | 4 | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| GPVI-mediated activation cascade | 3 | PIK3CA, PIK3CB, PIK3CG |
| Interleukin-3, Interleukin-5 and GM-CSF signaling | 3 | PIK3CA, PIK3CB, PIK3CD |
| RET signaling | 3 | PIK3CA, PIK3CB, PIK3CD |
| Interleukin receptor SHC signaling | 3 | PIK3CA, PIK3CB, PIK3CD |
| Regulation of signaling by CBL | 3 | PIK3CA, PIK3CB, PIK3CD |
| Signaling by CSF1 (M-CSF) in myeloid cells | 3 | PIK3CA, PIK3CB, PIK3CD |
| High laminar flow shear stress activates signaling by PIEZO1 and PECAM1:CDH5:KDR in endothelial cells | 3 | PIK3CA, PIK3CB, PIK3CD |
| PI3K Cascade | 2 | PIK3CA, PIK3CB |
| IRS-mediated signalling | 2 | PIK3CA, PIK3CB |
| Downstream signal transduction | 2 | PIK3CA, PIK3CB |
| PI3K/AKT activation | 2 | PIK3CA, PIK3CB |
| Signaling by ALK | 2 | PIK3CA, PIK3CB |
| Downstream TCR signaling | 2 | PIK3CA, PIK3CB |
| Role of phospholipids in phagocytosis | 2 | PIK3CA, PIK3CB |
| Tie2 Signaling | 2 | PIK3CA, PIK3CB |
| DAP12 signaling | 2 | PIK3CA, PIK3CB |
| Role of LAT2/NTAL/LAB on calcium mobilization | 2 | PIK3CA, PIK3CB |
| Nephrin family interactions | 2 | PIK3CA, PIK3CB |
| VEGFA-VEGFR2 Pathway | 2 | PIK3CA, PIK3CB |
| RAF/MAP kinase cascade | 2 | PIK3CA, PIK3CB |
| Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants | 2 | PIK3CA, PIK3CB |
| Signaling by PDGFRA extracellular domain mutants | 2 | PIK3CA, PIK3CB |
| Signaling by ALK fusions and activated point mutants | 2 | PIK3CA, PIK3CB |
| Signaling by LTK in cancer | 2 | PIK3CA, PIK3CB |
| Signaling by LTK | 2 | PIK3CA, PIK3CB |
| Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | 1 | PIK3CA |
| PI3K events in ERBB4 signaling | 1 | PIK3CA |
| Signaling by SCF-KIT | 1 | PIK3CA |
| GAB1 signalosome | 1 | PIK3CA |
| Signaling by cytosolic FGFR1 fusion mutants | 1 | PIK3CA |
| PI3K events in ERBB2 signaling | 1 | PIK3CA |
| G beta:gamma signalling through PI3Kgamma | 1 | PIK3CG |
| G alpha (q) signalling events | 1 | PIK3CA |
| Constitutive Signaling by EGFRvIII | 1 | PIK3CA |
| PI-3K cascade:FGFR1 | 1 | PIK3CA |
| PI-3K cascade:FGFR2 | 1 | PIK3CA |
| PI-3K cascade:FGFR3 | 1 | PIK3CA |
| PI-3K cascade:FGFR4 | 1 | PIK3CA |
| Signaling by FGFR2 in disease | 1 | PIK3CA |
| Signaling by FGFR4 in disease | 1 | PIK3CA |
| Signaling by FGFR1 in disease | 1 | PIK3CA |
| Signaling by FGFR3 in disease | 1 | PIK3CA |
| MET activates PI3K/AKT signaling | 1 | PIK3CA |
Dominant GO biological processes
| GO term | Targets |
|---|---|
| cell migration | 4 |
| phosphatidylinositol-3-phosphate biosynthetic process | 4 |
| phosphatidylinositol 3-kinase/protein kinase B signal transduction | 4 |
| phosphatidylinositol phosphate biosynthetic process | 4 |
| phosphatidylinositol-mediated signaling | 4 |
| lipid metabolic process | 4 |
| chemotaxis | 3 |
| positive regulation of endothelial cell migration | 3 |
| innate immune response | 3 |
| angiogenesis | 2 |
| platelet activation | 2 |
| vascular endothelial growth factor signaling pathway | 2 |
| T cell receptor signaling pathway | 2 |
| positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction | 2 |
| negative regulation of fibroblast apoptotic process | 2 |
Indications & clinical
Indications
3 approved indications. FDA phase 4, plus an anticancer drug’s labelled cancer uses (which ChEMBL often logs at phase 3).
| Indication | Phase | MONDO | EFO |
|---|---|---|---|
| neoplasm | 4 | MONDO:0005070 | EFO:0000616 |
| B-cell chronic lymphocytic leukemia | 4 | MONDO:0004948 | EFO:0000095 |
| follicular lymphoma | 4 | MONDO:0018906 | MONDO:0018906 |
15 diseases in clinical trials (phase 1–3, investigational — not approved indications). Highest ChEMBL trial phase per disease; a non-cancer approved use is occasionally logged at phase 3 here.
| Disease (in trials) | Phase | MONDO | EFO |
|---|---|---|---|
| non-Hodgkin lymphoma | 2 | MONDO:0018908 | EFO:0005952 |
| leukemia | 2 | MONDO:0005059 | EFO:0000565 |
| rheumatoid arthritis | 2 | MONDO:0008383 | EFO:0000685 |
| peripheral T-cell lymphoma, not otherwise specified | 2 | MONDO:0004964 | EFO:0000211 |
| head and neck squamous cell carcinoma | 2 | MONDO:0010150 | EFO:0000181 |
| hematopoietic and lymphoid system neoplasm | 2 | MONDO:0002334 | MONDO:0044881 |
| severe acute respiratory syndrome | 2 | MONDO:0005091 | MONDO:0100096 |
| asthma | 2 | MONDO:0004979 | MONDO:0004979 |
| lymphoma | 2 | MONDO:0005062 | EFO:0000574 |
| lymphoid leukemia | 2 | MONDO:0005402 | EFO:0004289 |
| liver disorder | 1 | MONDO:0005154 | EFO:0001421 |
| melanoma | 1 | MONDO:0005105 | EFO:0000756 |
| Sezary syndrome | 1 | MONDO:0017844 | EFO:1000785 |
| mycosis fungoides | 1 | MONDO:0009691 | EFO:1001051 |
| acute lymphoblastic leukemia | 1 | MONDO:0004967 | EFO:0000220 |
1 further indication record had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 55.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE1 | 20 |
| PHASE2 | 19 |
| PHASE1/PHASE2 | 8 |
| PHASE3 | 5 |
| Not specified | 2 |
| EARLY_PHASE1 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT06522737 | PHASE3 | RECRUITING | A Study of Duvelisib Versus Gemcitabine or Bendamustine in Participants With Relapsed/Refractory Nodal T Cell Lymphoma With T Follicular Helper (TFH) Phenotype |
| NCT02004522 | PHASE3 | COMPLETED | A Phase 3 Study of Duvelisib Versus Ofatumumab in Patients With Relapsed or Refractory CLL/SLL (DUO) |
| NCT02049515 | PHASE3 | COMPLETED | A Phase 3 Extension Study of Duvelisib and Ofatumumab in Participants With CLL/SLL Previously Enrolled in Study IPI-145-07 |
| NCT02204982 | PHASE3 | TERMINATED | Study of Duvelisib in Combination With Rituximab vs Rituximab in Subjects With Previously Treated Follicular Lymphoma |
| NCT02576275 | PHASE3 | WITHDRAWN | A Study of Duvelisib in Combination With Rituximab and Bendamustine vs Placebo in Combination With Rituximab and Bendamustine in Subjects With Previously-Treated Indolent Non-Hodgkin Lymphoma (BRAVURA) |
| NCT02158091 | PHASE1/PHASE2 | ACTIVE_NOT_RECRUITING | A Phase 1b/2 Study of IPI-145 Plus FCR in Previously Untreated, Younger Patients With CLL |
| NCT03534323 | PHASE1/PHASE2 | ACTIVE_NOT_RECRUITING | Duvelisib and Venetoclax in Relapsed or Refractory CLL or SLL or RS |
| NCT03961672 | PHASE2 | ACTIVE_NOT_RECRUITING | Intermittent Duvelisib Dosing in Treating Patients With Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma |
| NCT05675813 | PHASE1/PHASE2 | RECRUITING | Genotype-guided Treatment in Newly Diagnosed PTCL |
| NCT05976997 | PHASE2 | RECRUITING | Prospective, Single Arm, Single Center Study of Duvelisib Combined With Chidamide in the Treatment of Newly Diagnosed Peripheral T-cell Lymphoma (PTCL) |
| NCT06810778 | PHASE1/PHASE2 | RECRUITING | Duvelisib and Venetoclax in Patients With Relapsed or Refractory Peripheral T-cell Lymphoma (PTCL) |
| NCT07293403 | PHASE2 | NOT_YET_RECRUITING | Duvelisib Maintenance for the Treatment of Peripheral T-Cell Lymphomas |
| NCT01653756 | PHASE2 | COMPLETED | A Phase 2a, Efficacy and Safety Study of Duvelisib in Mild Asthmatic Subjects |
| NCT01851707 | PHASE2 | COMPLETED | A Double-Blind Study Evaluating Duvelisib in Subjects With Moderate to Severe Rheumatoid Arthritis and an Inadequate Response to Methotrexate Alone |
| NCT01882803 | PHASE2 | COMPLETED | A Study of Duvelisib in Participants With Refractory Indolent Non-Hodgkin Lymphoma |
| NCT02028039 | PHASE2 | WITHDRAWN | IPI-145 in Relapsed Refractory Acute Lymphoblastic Leukemia (ALL) |
| NCT02391545 | PHASE1/PHASE2 | TERMINATED | A Study of Duvelisib in Combination With Rituximab or Obinutuzumab in Subjects With Previously Untreated CD20+ Follicular Lymphoma (CONTEMPO) |
| NCT02605694 | PHASE2 | WITHDRAWN | Duvelisib With Rituximab vs R-CHOP in Subjects With Relapsed/Refractory Follicular Lymphoma (FRESCO) |
| NCT02711852 | PHASE2 | COMPLETED | A Long-term, Continued Treatment and Follow-up Study in Participants With Hematologic Malignancies Treated With Duvelisib (IPI-145) |
| NCT03370185 | PHASE2 | WITHDRAWN | Phase 2 Study of Duvelisib in Previously Treated Patients With Chronic Lymphocytic Leukemia /Small Lymphocytic Lymphoma |
| NCT03372057 | PHASE2 | COMPLETED | A Study of Duvelisib in Participants With Relapsed or Refractory Peripheral T-cell Lymphoma (PTCL) |
| NCT04038359 | PHASE2 | COMPLETED | A Phase 2 Study Comparing 2 Intermittent Dosing Schedules of Duvelisib in Participants With Indolent Non-Hodgkin Lymphoma |
| NCT04193293 | PHASE1/PHASE2 | TERMINATED | A Study of Duvelisib in Combination With Pembrolizumab in Head and Neck Cancer |
| NCT04209621 | PHASE2 | TERMINATED | Duvelisib for Ibrutinib-Resistant Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma |
| NCT04331119 | PHASE2 | TERMINATED | Duvelisib Maintenance After Autologous Stem Cell Transplant in T-Cell Lymphomas |
| NCT04372602 | PHASE2 | COMPLETED | Duvelisib to Combat COVID-19 |
| NCT04487886 | PHASE2 | COMPLETED | Duvelisib Ameliorates Manifestations of Pneumonia in Established Novel Coronavirus Infection (COVID-19) |
| NCT04688658 | PHASE1/PHASE2 | TERMINATED | Duvelisib in Combination With Nivolumab in Patients With Advanced Unresectable Melanoma |
| NCT04707079 | PHASE2 | UNKNOWN | A Safety and Efficacy Study of Duvelisib in Relapsed/Refractory Follicular Lymphoma |
| NCT04803201 | PHASE2 | SUSPENDED | Testing the Addition of Duvelisib or CC-486 to the Usual Treatment for Peripheral T-Cell Lymphoma |
| NCT05057247 | PHASE2 | COMPLETED | Duvelisib Plus Docetaxel In Recurrent/Metastatic HNSCC |
| NCT05508659 | PHASE1/PHASE2 | UNKNOWN | A Study of Duvelisib Combined With SG001 Injection in Patient With Advanced Solid Tumors |
| NCT04652960 | PHASE1 | ACTIVE_NOT_RECRUITING | Duvelisib and Nivolumab for the Treatment of Stage IIB-IVB Mycosis Fungoides and Sezary Syndrome |
| NCT05010005 | PHASE1 | RECRUITING | A Study of Ruxolitinib and Duvelisib in People With Lymphoma |
| NCT05044039 | PHASE1 | ACTIVE_NOT_RECRUITING | Duvelisib Following Chimeric Antigen Receptor T-Cell Therapy |
| NCT07001384 | PHASE1 | RECRUITING | A Study of Alectinib and Duvelisib in People With Anaplastic Lymphoma Kinase-Positive Anaplastic Large Cell Lymphoma (ALK+ALCL) |
| NCT01476657 | PHASE1 | TERMINATED | A Phase 1 Study of Duvelisib in Patients With Advanced Hematologic Malignancies |
| NCT01549106 | PHASE1 | COMPLETED | IPI-145 Single Ascending, Multiple Ascending, Food Effect and Drug-Drug-Interaction Study |
| NCT01836861 | PHASE1 | COMPLETED | IPI-145 ADME and Absolute Bioavailability Study |
| NCT01871675 | PHASE1 | COMPLETED | Study of IPI-145 in Combination With Rituximab or Bendamustine/Rituximab in Hematologic Malignancies |
| NCT01925911 | PHASE1 | COMPLETED | Phase 1 Study in Healthy Subjects to Evaluate the Effect of IPI-145 on the Pharmacokinetics of Midazolam |
| NCT01947777 | PHASE1 | COMPLETED | Phase 1 Study in Healthy Subjects to Evaluate the Effect of Rifampin on the Pharmacokinetics of IPI-145 |
| NCT02095587 | PHASE1 | COMPLETED | Duvelisib in Hepatically Impaired Subjects Compared to Healthy Subjects |
| NCT02292225 | PHASE1 | TERMINATED | Duvelisib With Obinutuzumab in Patients With CLL/SLL Previously Treated With a BTKi (SYNCHRONY) |
| NCT02307461 | PHASE1 | COMPLETED | Bioequivalence of Duvelisib and Food Effect on Pharmacokinetics of IPI-145 |
| NCT02598570 | PHASE1 | COMPLETED | Study Evaluating Duvelisib in Japanese Subjects With Relapsed or Refractory Lymphoma |
| NCT02640833 | PHASE1 | WITHDRAWN | A Study of Duvelisib and Venetoclax in Subjects With Relapsed or Refractory Chronic Lymphocytic Leukemia, Small Lymphocytic Lymphoma, or Indolent or Aggressive Non-Hodgkin Lymphoma, Who Have Not Previously Received a Bcl-2 or PI3K Inhibitor |
| NCT02783625 | PHASE1 | COMPLETED | Trial of Duvelisib in Combination With Either Romidepsin or Bortezomib in Relapsed/Refractory T-cell Lymphomas |
| NCT03892044 | PHASE1 | COMPLETED | Duvelisib and Nivolumab in Treating Patients With Richter Syndrome or Transformed Follicular Lymphoma |
| NCT04639843 | PHASE1 | WITHDRAWN | Doxorubicin, CC-(486) (5-azacitidine), Romidepsin, and Duvelisib (hARD) for T-cell Lymphoma |
| NCT04836832 | PHASE1 | WITHDRAWN | Acalabrutinib and Duvelisib for the Treatment of Relapsed/Refractory Indolent Non-Hodgkin Lymphoma |
| NCT05065866 | PHASE1 | COMPLETED | Duvelisib in Combination With BMS-986345 in Lymphoid Malignancy |
| NCT04890236 | EARLY_PHASE1 | COMPLETED | Duvelisib Exposure to Enhance Immune Profiles of T Cells in Patients With Recurrent or Refractory Diffuse Large B-Cell Lymphoma, DEEP T CELLS Study |
| NCT05923502 | Not specified | NOT_YET_RECRUITING | (CHANT)Real World Study of Duvelisib in the Treatment of Non-Hodgkin’s Lymphoma (NHL) |
| NCT04342117 | Not specified | TERMINATED | Observational Trial of Real-World Treatment Utilization and Effectiveness of PI3K-inhibitors in CLL/SLL and FL |
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No CPIC/DPWG dosing guideline or drug-level clinical/variant annotations in PharmGKB for this molecule.
Related molecules
Related molecules
Molecules sharing ≥1 of this drug’s curated primary targets, merged from two biobtree sources and ranked by shared-target count, then clinical phase: ChEMBL clinical-stage candidates (development phase ≥2) and PubChem drug-class bioactivity (approved / known drugs acting on the target). Deduplicated by drug name; the drug’s own salt forms are excluded. Note: for a drug with few primary targets a shared-target match can reflect off-target / promiscuous binding rather than the same therapeutic mechanism — the phase ordering surfaces bona-fide therapeutics first.
72 molecules share ≥1 primary target. Top 72 by shared-target count:
| Molecule | Source | Status | Shared targets |
|---|---|---|---|
| CRIZOTINIB | ChEMBL + PubChem | Phase 4 (approved) | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| IDELALISIB | ChEMBL + PubChem | Phase 4 (approved) | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| INAVOLISIB | ChEMBL + PubChem | Phase 4 (approved) | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| ALPELISIB | ChEMBL | Phase 4 (approved) | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| COPANLISIB | ChEMBL | Phase 4 (approved) | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| LENIOLISIB | ChEMBL | Phase 4 (approved) | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| BUPARLISIB | ChEMBL | Phase 3 | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| DACTOLISIB | ChEMBL | Phase 3 | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| GEDATOLISIB | ChEMBL | Phase 3 | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| LESTAURTINIB | ChEMBL | Phase 3 | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| TASELISIB | ChEMBL | Phase 3 | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| AMG-319 | ChEMBL | Phase 2 | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| APITOLISIB | ChEMBL | Phase 2 | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| AZD-6482 | ChEMBL | Phase 2 | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| BGT-226 FREE BASE | ChEMBL | Phase 2 | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| BIMIRALISIB | ChEMBL | Phase 2 | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| EGANELISIB | ChEMBL | Phase 2 | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| FIMEPINOSTAT | ChEMBL | Phase 2 | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| IZORLISIB | ChEMBL | Phase 2 | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| NEMIRALISIB | ChEMBL | Phase 2 | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| OMIPALISIB | ChEMBL | Phase 2 | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| ONATASERTIB | ChEMBL | Phase 2 | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| PAXALISIB | ChEMBL | Phase 2 | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| PF-04691502 | ChEMBL | Phase 2 | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| PICTILISIB | ChEMBL | Phase 2 | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| PILARALISIB | ChEMBL | Phase 2 | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| ROGINOLISIB | ChEMBL | Phase 2 | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| SAMOTOLISIB | ChEMBL | Phase 2 | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| SAPANISERTIB | ChEMBL | Phase 2 | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| SERABELISIB | ChEMBL | Phase 2 | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| TG100-115 | ChEMBL | Phase 2 | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| VISTUSERTIB | ChEMBL | Phase 2 | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| VOXTALISIB | ChEMBL | Phase 2 | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| ZSTK-474 | ChEMBL | Phase 2 | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| Afatinib | PubChem | Approved | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| Pazopanib | PubChem | Approved | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| Selumetinib | PubChem | Approved | PIK3CA, PIK3CB, PIK3CD, PIK3CG |
| SUNITINIB | ChEMBL | Phase 4 (approved) | PIK3CA, PIK3CD, PIK3CG |
| DEZAPELISIB | ChEMBL | Phase 2 | PIK3CB, PIK3CD, PIK3CG |
| QUISINOSTAT | ChEMBL | Phase 2 | PIK3CA, PIK3CB, PIK3CD |
| RISOVALISIB | ChEMBL | Phase 2 | PIK3CA, PIK3CB, PIK3CD |
| SONOLISIB | ChEMBL | Phase 2 | PIK3CA, PIK3CD, PIK3CG |
| Gefitinib | PubChem | Approved | PIK3CB, PIK3CD, PIK3CG |
| DASATINIB | ChEMBL | Phase 4 (approved) | PIK3CA, PIK3CD |
| FEDRATINIB | ChEMBL | Phase 4 (approved) | PIK3CA, PIK3CG |
| UMBRALISIB | ChEMBL | Phase 4 (approved) | PIK3CD, PIK3CG |
| RESVERATROL | ChEMBL | Phase 3 | PIK3CA, PIK3CB |
| ACALISIB | ChEMBL | Phase 2 | PIK3CD, PIK3CG |
| AMDIZALISIB | ChEMBL | Phase 2 | PIK3CD, PIK3CG |
| AZD-8154 | ChEMBL | Phase 2 | PIK3CA, PIK3CD |
| BI-2536 | ChEMBL | Phase 2 | PIK3CA, PIK3CD |
| GSK-2636771 | ChEMBL | Phase 2 | PIK3CB, PIK3CD |
| OSI-027 | ChEMBL | Phase 2 | PIK3CA, PIK3CG |
| SELETALISIB | ChEMBL | Phase 2 | PIK3CD, PIK3CG |
| TENALISIB | ChEMBL | Phase 2 | PIK3CD, PIK3CG |
| BELINOSTAT | ChEMBL | Phase 4 (approved) | PIK3CA |
| CAFFEINE | ChEMBL | Phase 4 (approved) | PIK3CD |
| MIDOSTAURIN | ChEMBL | Phase 4 (approved) | PIK3CA |
| ROMIDEPSIN | ChEMBL | Phase 4 (approved) | PIK3CA |
| THEOPHYLLINE | ChEMBL | Phase 4 (approved) | PIK3CD |
| EPIGALOCATECHIN GALLATE | ChEMBL | Phase 3 | PIK3CA |
| IPATASERTIB | ChEMBL | Phase 3 | PIK3CA |
| PARSACLISIB | ChEMBL | Phase 3 | PIK3CD |
| POVORCITINIB | ChEMBL | Phase 3 | PIK3CD |
| QUERCETIN | ChEMBL | Phase 3 | PIK3CG |
| BERZOSERTIB | ChEMBL | Phase 2 | PIK3CA |
| CC-115 | ChEMBL | Phase 2 | PIK3CA |
| LINPERLISIB | ChEMBL | Phase 2 | PIK3CD |
| MMV-048 | ChEMBL | Phase 2 | PIK3CA |
| NARAZACICLIB | ChEMBL | Phase 2 | PIK3CD |
| R-406 | ChEMBL | Phase 2 | PIK3CD |
| RAFOXANIDE | ChEMBL | Phase 2 | PIK3CA |
Related Atlas pages
- Genes: PIK3CA, PIK3CB, PIK3CD, PIK3CG
- Indicated for: neoplasm, B-cell chronic lymphocytic leukemia, follicular lymphoma
- In clinical trials for: non-Hodgkin lymphoma, leukemia, rheumatoid arthritis, peripheral T-cell lymphoma, not otherwise specified, head and neck squamous cell carcinoma, hematopoietic and lymphoid system neoplasm, severe acute respiratory syndrome, asthma, lymphoma, lymphoid leukemia
- Drugs: Crizotinib, Idelalisib, Inavolisib, Alpelisib, Copanlisib, Leniolisib, Buparlisib, Dactolisib, Gedatolisib, Lestaurtinib, Taselisib, Afatinib, Pazopanib, Selumetinib, Sunitinib, Gefitinib, Dasatinib, Fedratinib, Umbralisib, Resveratrol, Belinostat, Caffeine, Midostaurin, Romidepsin, Theophylline, Epigalocatechin Gallate, Ipatasertib, Parsaclisib, Povorcitinib, Quercetin