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statement

# **Following the D2T RA clinical success, the risk discount is reduced from 50% to 40%, leading to a revaluation of IMVT-1402.**

A statement by report author. Statements are as reported by the cited publishers — not verified by DecisionGateway.

> *D2T RA 임상 성공에 따라 위험 할인을 기존 50%에서 40%로 축소하며 IMVT-1402의 가치 재평가*

companyreportPublished 2026-11-10 [ Read source](https://t.me/companyreport/116013)

## **Related claims**

[**Immunovant's Phase 2b trial of IMVT-1402 in difficult-to-treat rheumatoid arthritis (D2T RA) demonstrated excellent efficacy and safety, securing the validity of the development strategy.**report author · statement](https://dgw.tmarket.io/claims/01a1d4b6-f731-7ec4-848f-6e8b93480486) [**In the D2T RA Phase 2b Period 2 results, the 600mg continuous dosing group achieved statistical significance (p-value), a surprise exceeding market expectations.**report author · statement](https://dgw.tmarket.io/claims/01a1d4b6-f6d1-7aec-8105-c4689a803513) [**IMVT-1402 is the first clinical case to demonstrate that continuous high-dose dosing is possible without the hypercholesterolemia concerns seen with Batoclimab.**report author · statement](https://dgw.tmarket.io/claims/01a1d4b6-f6f1-7ada-9bde-36834d645c3f) [**Developers removed version 4 transactions, the only means of spending those coins, to eliminate old and complex verification code and denial-of-service (DoS) risk.**AIXBT · statement](https://dgw.tmarket.io/claims/01a1d6b4-ce70-7e81-8cdc-359ef9cf7cc4) [**The 600mg continuous dosing group recorded an ACR20 value of 92.5%, demonstrating excellent efficacy in absolute terms.**report author · statement](https://dgw.tmarket.io/claims/01a1d4b6-f6e3-7be5-ab83-bf2b785418ad) [**The trade has a 3:1 risk-reward ratio.**derstandardat · statement](https://dgw.tmarket.io/claims/01a1d020-ce8c-7320-ac71-4f5ae218ee11)

[All claims](https://dgw.tmarket.io/claims)

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```

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