NKX019 + Fludarabine + Cyclophosphamide

Phase 1/2Recruiting
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Interest: 29/100
29
Hype Score

Development Stage

Pre-clinical
2
Phase 1
3
Phase 2
4
Phase 3
5
Approved
Indication / Disease

Systemic Sclerosis

Conditions

Systemic Sclerosis, Idiopathic Inflammatory Myopathies, Antineutrophil Cytoplasmic Antibody-Associated Vasculitis

Trial Timeline

Nov 4, 2024 → Oct 1, 2028

About NKX019 + Fludarabine + Cyclophosphamide

NKX019 + Fludarabine + Cyclophosphamide is a phase 1/2 stage product being developed by Nkarta for Systemic Sclerosis. The current trial status is recruiting. This product is registered under clinical trial identifier NCT06733935. Target conditions include Systemic Sclerosis, Idiopathic Inflammatory Myopathies, Antineutrophil Cytoplasmic Antibody-Associated Vasculitis.

What happened to similar drugs?

10 of 20 similar drugs in Systemic Sclerosis were approved

Approved (10) Terminated (4) Active (7)
Baricitinib + CyclophosphamideEli LillyApproved
Rosuvastatin + SimvastatinAstraZenecaApproved
AnifrolumabAstraZenecaApproved
EfalizumabMerckApproved
AmbrisentanGilead SciencesApproved
BMS-986165Bristol Myers SquibbApproved
versus hydroxychloroquineSanofiApproved

Hype Score Breakdown

Clinical
9
Activity
15
Company
5
Novelty
0
Community
0

Clinical Trials (1)

NCT IDPhaseStatus
NCT06733935Phase 1/2Recruiting

Competing Products

20 competing products in Systemic Sclerosis

See all competitors
ProductCompanyStageHype Score
Tabalumab Auto-Injector + Tabalumab Prefilled SyringeEli LillyPhase 3
32
Baricitinib + PlaceboEli LillyPhase 2
35
MRA(Tocilizumab) + placeboChugai PharmaceuticalPhase 3
40
MRA(Tocilizumab)Chugai PharmaceuticalPhase 3
40
MRA(Tocilizumab)Chugai PharmaceuticalPhase 3
40
DS-7011a + PlaceboDaiichi SankyoPhase 1
29
DS-7011a + PlaceboDaiichi SankyoPhase 1/2
32
Bocidelpar + PlaceboAstellas PharmaPhase 1
21
Parenteral micafungin application + Other parenteral antifungal drugsAstellas PharmaPre-clinical
26
MicafunginAstellas PharmaPhase 2
35
E6742EisaiPhase 1/2
32
KHK4827Kyowa KirinPhase 1
29
KHK4827 + PlaceboKyowa KirinPhase 3
40
Baricitinib + PlaceboEli LillyPhase 3
40
Baricitinib + CyclophosphamideEli LillyApproved
47
Baricitinib + PlaceboEli LillyPhase 3
32
LY2127399 + Placebo every 2 weeks + Placebo every 4 weeks + Standard of CareEli LillyPhase 3
40
LY3361237 + PlaceboEli LillyPhase 2
27
LY2127399 + PlaceboEli LillyPhase 3
32
LY3361237 + PlaceboEli LillyPhase 1
29