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Medical Information
  • GILEAD and the GILEAD logo are trademarks of Gilead Sciences, Inc. KITE and the KITE logo are trademarks of Kite Pharma, Inc. © 2023 Gilead Sciences, Inc. All rights reserved. US-UNBP-2480 12/23

Our pipeline.

Active and planned clinical trials

Click row, filter menu or scientific focus key color to view available clinical trial study designs.

The safety and efficacy of these investigational agents and/or uses have not been established. There is no guarantee that they will become commercially available.

Our scientific focus areas target:
Tumor-intrinsic cell death Immune-mediated tumor killing Tumor-permissive microenvironment
TUMOR TYPE RESEARCH AREA Molecule(s)
PHASE 1 PHASE 2 PHASE 3
Hematological malignancies 1L unfit AML (ENHANCE-3)a Magrolimab + venetoclax + azacitidine NCT05079230
R/R DLBCL (5F9003)b Magrolimab combinations NCT02953509 1b/2
AML multicohort Magrolimab combinations NCT04778410
R/R MM Magrolimab combinations NCT04892446
MDS/AML multicohort (5F9005) Magrolimab + azacitidine NCT03248479            1b
2L+ high-risk FL (ZUMA-22) Axicabtagene ciloleucel NCT05371093
1L high-risk LBCL (ZUMA-23) Axicabtagene ciloleucel NCT05605899
2L LBCL outpatient (ZUMA-24) Axicabtagene ciloleucel NCT05459571
Rare B-cell malignancies (ZUMA-25) Brexucabtagene autoleucel NCT05537766
R/R Pediatric ALL/NHL (ZUMA-4) Brexucabtagene autoleucel NCT02625480
R/R MM (iMMagine-1)c Anitocabtagene autoleucel NCT05396885
R/R AML KITE-222 NCT04789408
R/R BCL KITE-363 or KITE-753 NCT04989803
Breast 1L mTNBC, PD-L1- (ASCENT-03) Sacituzumab govitecan NCT05382299
1L mTNBC, PD-L1+ (ASCENT-04)d Sacituzumab govitecan + pembrolizumab NCT05382286
Adjuvant TNBC (ASCENT-05)e Sacituzumab govitecan + pembrolizumab NCT05633654
1L HR+/HER2- chemo-naïve mBC (ASCENT-07) Sacituzumab govitecan NCT05840211
2L+ HR+/HER2- mBC (EVER-132-002)f Sacituzumab govitecan (SG) NCT04639986
2L+ mTNBC (ASCENT-J02) Sacituzumab govitecan NCT05101096 1/2
1-2L mTNBC (ELEVATE TNBC)g Magrolimab + chemotherapy/SG combinations NCT04958785
GU 2L+ mUC (TROPiCS-04) Sacituzumab govitecan NCT04527991
1L+ mUC (TROPHY U-01) Sacituzumab govitecan + combinations NCT03547973
Lung and Thoracic 2-3L mNSCLC (EVOKE-01) Sacituzumab govitecan NCT05089734
1L mNSCLC, PD-L1+, TPS≥50% (EVOKE-03)d,h Sacituzumab govitecan + pembrolizumab NCT05609968
1L mNSCLC (STAR-121)i Domvanalimab + zimberelimab + chemotherapy NCT05502237
1L mNSCLC, PD-L1+, TPS≥50% (ARC-10)i,j Domvanalimab + zimberelimab NCT04736173
Stage 3 NSCLC (PACIFIC-8) i,k,l Domvanalimab + durvalumab NCT05211895
1L mNSCLC (EVOKE-02)d Sacituzumab govitecan ± pembrolizumab ± chemo NCT05186974
1L mNSCLC (ARC-7)i,m Domvanalimab + zimberelimab + etrumadenant NCT04262856
1-2L mNSCLC (VELOCITY-Lung)i Dom + zim + etruma + SG combinations NCT05633667
1-2L mNSCLC (EDGE-Lung)i Dom + zim + quemli + chemotherapy combinations NCT05676931
1-3L mHNSCC (ELEVATE HNSCC)n Magrolimab + chemo/IO combinations NCT04854499
gastrointestinal 1L upper GI malignancies (STAR-221)i,o,p Domvanalimab + zimberelimab + chemotherapy NCT05568095
1-2L upper GI (ARC-21/EDGE-Gastric)i,q Domvanalimab + zimberelimab + chemotherapy NCT05329766
2L+ mCRC (ARC-9)i,r Etrumadenant + zimberelimab combinations NCT04660812 1b/2
2L mCRC (ELEVATE CRC)s Magrolimab combinations NCT05330429
1-2L mPDAC (ARC-8)i,t Quemliclustat + zimberelimab + chemo NCT04104672
Other solid tumors Solid tumors (EVER-132-003) Sacituzumab govitecan NCT05119907
Solid tumor basket study (TROPiCS-03)u Sacituzumab govitecan NCT03964727
Solid tumors (ELEVATE Lung & UC) Magrolimab + chemo NCT04827576
Advanced/metastatic solid tumor (hepatic impairment) v Sacituzumab govitecan NCT04617522
Solid tumors (ARC-12)i AB308 + zimberelimab NCT04772989
Solid tumors GS-9716 (MCL-1) + chemo or SG NCT05006794
Solid tumors GS-1811 (CCR8) + zim NCT05007782
Solid tumors GS-4528 (IL2 variant) + zim NCT05840224
Solid tumors GS-0201 (PARPi)
Planned
Solid tumors GS-9911 (DGKα)
Planned

Optionable Partner Programs 1,w

Agenus

1 clinical stage program
Solid tumors

Arcus

1 clinical stage program
PK study

Tizona

1 clinical stage program
Advanced cancers

MacroGenics

1 clinical stage program
Advanced cancers


Targets

Sacituzumab govitecan GS-9716 Axicabtagene ciloleucel, Brexucabtagene autoleucel Magrolimab KITE-363, KITE-753 KITE-222 Anito-cel Zimberelimab Domvanalimab, AB308 GS-4528 Etrumadenant GS-1811 Quemliclustat
TROP2 MCL-1 CD19 CD47 CD19/20 CLL1 BCMA PD-1 TIGIT IL2 variant A2AR/A2BR CCR8 CD73

The safety and efficacy of these investigational agents and/or uses have not been established. There is no guarantee that they will become commercially available.

aFor participants with previously untreated AML who are ineligible for intensive chemotherapy. bPatient population includes those with R/R NHL, including R/R DLBCL. ciMMagine-1 is being codeveloped with Arcellx. dIn collaboration with Merck. eIn collaboration with Alliance Foundation Trials, LLC. fA Phase 3 Asian Study of Sacituzumab Govitecan Versus Treatment of Physician's Choice (TPC) in Subjects With Hormonal Receptor-positive (HR+)/Human Epidermal Growth Factor Receptor 2 Negative (HER2-) Metastatic Breast Cancer (MBC) Who Have Failed at Least 2 Prior Chemotherapy Regimens. gMagro + chemo and Magro + SG. hEVOKE-03 is being operationalized by Merck. iIn collaboration with Arcus Biosciences. jARC-10: Dom + Zim vs Pembro. kPACIFIC-8: Durva + Dom vs Durva + placebo. lIn collaboration with AstraZeneca. mARC-7: Zim ± Dom ± Etruma. nMagro + Pembro + chemo and Pembro + chemo and Magro + Zim + chemo. oSTAR-221 is being operationalized by Arcus Biosciences. pSTAR-221: Dom + Zim + FOLFOX vs Nivo + FOLFOX. qARC-21/EDGE-Gastric: (1L) Dom + Zim + chemo, Zim + chemo and (2L) Dom + Zim, Zim + Quemli. rARC-9: Etruma + Zim + FOLFOX vs FOLFOX, Etruma + Zim + FOLFOX vs Rego, and Etruma + Zim + Quemli. sMagro + Bev + FOLFIRI. tARC-8: Quemli + Zim + Gem/Nab-pac. umNSCLC, mSCLC, mHNSCC, mEC. vPatient population includes those with moderate hepatic impairment. wSelected programs listed are optionable partner programs. Gilead has not opted into these programs unless otherwise noted.

1L, first line; 2L, second line; 3L, third line; A2aR/A2bR, adenosine 2a receptor/adenosine 2b receptor; ALL, acute lymphoblastic leukemia; AML, acute myeloid leukemia; Bev, bevacizumab; BC, breast cancer; BCL, B-cell lymphoma; CAR-T ddBCMA, autologous anti-B-cell maturation antigen (BCMA) Chimeric Antigen Receptor (CAR)T-cell therapy; CCR8, chemokine receptor 8; CD19/20/47/73, cluster of differentiation 19/20/47/73; Chemo, chemotherapy; CLL-1, C-type lectin-like molecule-1; CRC, colorectal cancer; DLBCL, diffuse large B-cell lymphoma; Doce, docetaxel; DGKα, diacylglycerol kinase alpha; Dom, domvanalimab; Durva, durvalumab; EC, endometrial cancer; Etruma, etrumadenant; FL, follicular lymphoma; FOLFIRI, FOLinic acid-Fluorouracil-IRInotecan regimen; FOLFOX, FOLinic acid-Fluororuracil-OXaliplatin regimen; Gem/Nab-pac, gemcitabine/nab-paclitaxel; GI, gastrointestinal; GU, genitourinary; HNSCC, head and neck squamous cell carcinoma; IO, immuno-oncology; ITIM, immunoreceptor tyrosine-based inhibitory motif; LBCL, large B-cell lymphoma; m, metastatic; Magro, magrolimab; MCL-1, myeloid cell leukemia-1; MM, multiple myeloma; NCT, national clinical trial; Nivo, nivolumab; NHL, non-Hodgkin lymphoma; NSCLC, non-small cell lung cancer; PARPi, poly (adenosine diphosphate [ADP]) ribose polymerase (PARP) inhibitor; Pembro, pembrolizumab; PD-1, programmed cell death protein 1; PD-L1, programmed death-ligand 1; PDAC, pancreatic ductal adenocarcinoma; PK, pharmacokinetics; Quemli, quemliclustat; Rego, regorafenib; R/R, relapsed/refractory; SG, sacituzumab govitecan; TIGIT, T cell immunoreceptor with immunoglobulin and ITIM domains; TNBC, triple-negative breast cancer; TROP2, trophoblast cell-surface antigen 2; UC, urothelial cancer; Zim, zimberelimab.

1. Gilead Sciences Inc. Third Quarter 2023 Earnings Call. November 7, 2023. Available at: https://s29.q4cdn.com/585078350/files/doc_financials/2023/q3/GILD-Q323-Earnings-Presentation-7-November-2023.pdf 2. ClinicalTrials.gov website.