Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://clinicaltrials.gov/ct2/show/NCT03427151
200 mcg of IPP-201101 (FORIGERIMOD) will be administered subcutaneously every 4 weeks for 24 weeks.
Route of Administration:
Other
| Substance Class |
Protein
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| Protein Sub Type | |
| Sequence Type | COMPLETE |
| Record UNII |
YU54FAR97X
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| Record Status |
Validated (UNII)
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| Code System | Code | Type | Description | ||
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C170004
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1160237-55-7
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100000175236
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XX-42
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CHEMBL2103866
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YU54FAR97X
Created by
admin on Mon Mar 31 21:00:44 GMT 2025 , Edited by admin on Mon Mar 31 21:00:44 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
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STARTING MATERIAL -> INGREDIENT |
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PARENT -> SALT/SOLVATE |
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ACTIVE MOIETY |
Agent Modifications
| Modification Process | Modification Role | Modification Type | Amount | Fragment Name | Fragment ID |
|---|---|---|---|---|---|
| ACETYLATION | CHEMICAL | Acetic acid | Q40Q9N063P |
Structural Modifications
| Modification Type | Location Site | Location Type | Residue Modified | Extent | Fragment Name | Fragment Approval |
|---|---|---|---|---|---|---|
| AMINO ACID SUBSTITUTION | [1_10] | SERINE | DEXFOSFOSERINE | VI4F0K069V |
| Name | Property Type | Amount | Referenced Substance | Defining | Parameters | References |
|---|---|---|---|---|---|---|
| MOL_WEIGHT:NUMBER(CALCULATED) | CHEMICAL |
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| Molecular Formula | CHEMICAL |
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