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Shenqi Sherong Pill

Phase 3

Cervical Spondylotic Myelopathy | Small molecule | Other |HUTCHMED (China) Limited|Trials Updated: Apr 23, 2026

Shenqi Sherong Pill development status

Highest phase Phase 3
Registered trials 1 across 1 sponsor since Apr 2024

Success Probability

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Market & Valuation

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Trial Design

RandomizedDouble-BlindPLACEBO_CONTROLLED
Total Trials1
Total Enrollment428

FDA Designations

No designations recorded

Shenqi Sherong Pill clinical trials

Shenqi Sherong Pill · 1 trial · 1 indication

Phase 3 1
NCT06377072Efficacy and Safety of Shenqi Sherong Pill in Participants With Cervical Spondylotic MyelopathyCervical Spondylotic Myelopathy
COMPLETED428 Analytics
PHASE3COMPLETED
Efficacy and Safety of Shenqi Sherong Pill in Participants With Cervical Spondylotic Myelopathy
Cervical Spondylotic MyelopathyUnlock trial analytics

Study Endpoints

Primary Endpoints

Change in Modified Japanese Orthopaedic Association (mJOA) score
42±2 days

Change in Modified Japanese Orthopaedic Association (mJOA) score (on a scale from 0 to 18, with lower scores indicating greater disability) from baseline at Day 42 after administration; the mJOA which is a clinician administered scale to evaluate four clinical dimensions; motor dysfunction score for upper and lower extremities, sensation loss and sphincter dysfunction.

Secondary Endpoints

Change in mJOA score
14±2 days, 28±2 days, 56±2 days
Change in sensation of mJOA score
14±2 days, 28±2 days, 42±2 days or 56±2 days
Changes in pain or stiffness score for neck and shoulder
14±2 days, 28±2 days, 42±2 days or 56±2 days
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Study Design & Arms

AllocationRANDOMIZED
MaskingDOUBLE
ModelPARALLEL
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
Shenqi Sherong PillEXPERIMENTAL6g per bag
PlaceboPLACEBO_COMPARATOR6g per bag

Interventions

NameTypeDescription
Shenqi Sherong PillDRUGtwo bags each time, three times a day at half an hour after breakfast, lunch and dinner for 6 weeks
PlaceboDRUGtwo bags each time, three times a day at half an hour after breakfast, lunch and dinner for 6 weeks
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Eligibility Criteria

Age Range18 Years to 75 Years
SexALL
Healthy VolunteersNo
Study Sites1

Inclusion Criteria: Participants can only be selected if they meet all the inclusion criteria 1. Age 18-75 years old (including 18 and 75 years old), gender unlimited; 2. Accord with Western medicine diagnosis standards of Cervical Spondylotic Myelopathy; 3. Accord with Chinese medicine diagnosis ...

Countries:China
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Frequently asked questions about Shenqi Sherong Pill

What is Shenqi Sherong Pill?

Shenqi Sherong Pill is an investigational small molecule therapeutic being developed by HUTCHMED (China) Limited for cervical spondylotic myelopathy, a spinal cord condition caused by compression in the neck. It has been studied in a Phase 3 clinical trial and is not described as approved.

What is Shenqi Sherong Pill used for?

Shenqi Sherong Pill is being developed for the treatment of cervical spondylotic myelopathy. This condition involves compression of the spinal cord in the cervical spine. The drug has been evaluated in a Phase 3 trial in participants with this indication.

Who makes Shenqi Sherong Pill?

Shenqi Sherong Pill is developed by HUTCHMED (China) Limited, which trades under the ticker HCM. The company is the sponsor of the clinical program for this asset.

What phase is Shenqi Sherong Pill in?

Shenqi Sherong Pill has completed a Phase 3 clinical trial. It is an investigational therapy and is not described as approved. The Phase 3 study has been completed, and no active trials are currently listed for this drug.

What clinical trials is Shenqi Sherong Pill in?

Shenqi Sherong Pill has been studied in one Phase 3 clinical trial, NCT06377072, titled "Efficacy and Safety of Shenqi Sherong Pill in Participants With Cervical Spondylotic Myelopathy." The trial enrolled 428 participants in China, was randomized, double-blind, and placebo-controlled, and has been completed.