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Solid and Hematological Malignancies

0
Pipeline Programs
4
Companies
2
Clinical Trials
0
Approved Products

Pipeline by Development Stage

Preclinical
Phase 1
Phase 1/2
Phase 2
Phase 2/3
Phase 3
On Market
0
0
0
0
0
0
0
Early DiscoveryClinical DevelopmentMarket

Drug Modality Breakdown

Cell Therapy
267%
Small Molecule
133%
+ 1 programs with unclassified modality

Competitive Landscape

4 companies ranked by most advanced pipeline stage

Gilead Sciences
Gilead SciencesFOSTER CITY, CA
1 program
Axicabtagene CiloleucelN/ACell Therapy
Kite Pharma
Kite PharmaCA - El Segundo
1 program
Axicabtagene CiloleucelN/ACell Therapy1 trial
Active Trials
NCT05041309Enrolling By Invitation1,000Est. Dec 2040
Adaptimmune Therapeutics
Adaptimmune TherapeuticsPA - Philadelphia
1 program
Genetically engineered T Cell ReceptorsN/A1 trial
Active Trials
NCT03391791Terminated2Est. Jul 2018
Parexel
ParexelMA - Boston
1 program
CapivasertibPHASE_1Small Molecule

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
2027
2028
2029
2030
2031
Kite PharmaAxicabtagene Ciloleucel
Adaptimmune TherapeuticsGenetically engineered T Cell Receptors

Clinical Trials (2)

Total enrollment: 1,002 patients across 2 trials

NCT05041309Kite PharmaAxicabtagene Ciloleucel

Long-term Follow-up Study for Participants of Kite-Sponsored Interventional Studies Treated With Gene-Modified Cells

Start: Dec 2021Est. completion: Dec 20401,000 patients
N/AEnrolling By Invitation
NCT03391791Adaptimmune TherapeuticsGenetically engineered T Cell Receptors

Long Term Follow up of Subjects Exposed to Genetically Engineered T Cell Receptors

Start: Feb 2018Est. completion: Jul 20182 patients
N/ATerminated

Phase Legend

PreclinicalLab & animal studies
Phase 1Safety & dosing
Phase 2Efficacy testing
Phase 3Large-scale trials
On MarketApproved & available

Key Insights

Cell Therapy is the dominant modality (67% of programs)
4 companies competing in this space

The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.