the low-dose group (1.5 g/day) or the standard-dose group (4 g/day)

Pre-clinicalRecruiting
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23
Hype Score

Development Stage

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

Hyperphosphatemia

Conditions

Hyperphosphatemia

Trial Timeline

Dec 21, 2023 โ†’ Dec 31, 2025

About the low-dose group (1.5 g/day) or the standard-dose group (4 g/day)

the low-dose group (1.5 g/day) or the standard-dose group (4 g/day) is a pre-clinical stage product being developed by Kyowa Kirin for Hyperphosphatemia. The current trial status is recruiting. This product is registered under clinical trial identifier NCT06206135. Target conditions include Hyperphosphatemia.

Hype Score Breakdown

Clinical
5
Activity
2
Company
10
Novelty
2
Community
1

Clinical Trials (1)

NCT IDPhaseStatus
NCT06206135Pre-clinicalRecruiting

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ASP1585Astellas PharmaPhase 2
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KHK7791 + PlacebpKyowa KirinPhase 2
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KHK7791Kyowa KirinPhase 2
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KHK7791 + PlaceboKyowa KirinPhase 3
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KHK7791 + PlaceboKyowa KirinPhase 3
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KHK7791Kyowa KirinPhase 3
77
KHK7791 + PlaceboKyowa KirinPhase 2
52
KHK7791Kyowa KirinPhase 3
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SBR759 + Sevelamer HCl + SBR759 + Sevelamer HClNovartisPhase 2
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SBR759A + SBR759A + SBR759A + SBR759A + SBR759ANovartisPhase 3
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PA21Kissei PharmaceuticalPhase 3
76
Placebo + Sevelamer Carbonate (GZ419831)SanofiPhase 3
76
Placebo + Sevelamer carbonateSanofiPhase 2
51
Lanthanum Carbonate (Fosrenol, BAY77-1931) - chewable tabletBayerPre-clinical
20
Lanthanum Carbonate (Fosrenol, BAY77-1931)BayerPre-clinical
20
Lanthanum Carbonate (BAY77-1931)BayerPhase 2
49