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†’ Jan 30, 2026

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

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 NCT06186934. Target conditions include Hyperphosphatemia.

Hype Score Breakdown

Clinical
5
Activity
2
Company
10
Novelty
2
Community
1

Clinical Trials (1)

NCT IDPhaseStatus
NCT06186934Pre-clinicalRecruiting

Competing Products

20 competing products in Hyperphosphatemia

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EOS789 + Placebo + RenvelaChugai PharmaceuticalPhase 1
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DS-2330b PIB + Placebo + Sevelamer + DS-2330b TabletDaiichi SankyoPhase 1
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ASP1585 + Placebo + Sevelamer hydrochlorideAstellas PharmaPhase 2
52
ASP1585Astellas PharmaPhase 2
52
KHK7791 + PlacebpKyowa KirinPhase 2
52
KHK7791Kyowa KirinPhase 2
52
KHK7791 + PlaceboKyowa KirinPhase 3
77
the low-dose group (1.5 g/day) or the standard-dose group (4 g/day)Kyowa KirinPre-clinical
23
KHK7791 + PlaceboKyowa KirinPhase 3
77
KHK7791Kyowa KirinPhase 3
77
KHK7791 + PlaceboKyowa KirinPhase 2
52
KHK7791Kyowa KirinPhase 3
77
SBR759 + Sevelamer HCl + SBR759 + Sevelamer HClNovartisPhase 2
52
SBR759A + SBR759A + SBR759A + SBR759A + SBR759ANovartisPhase 3
77
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