> Trialight public data. Index of pages: https://trialight.com/llms.txt
> Web page: https://trialight.com/data/asset/ebdarokimab-45f8668d-cb15-4f87-8ef8-ba945179af66
> Record changed: 2026-11-04

# Ebdarokimab

Highest phase reached

Phase 3

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL4650437)

Drug type

Antibody

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL4650437)

## Development status

**Listing at source**

Listed

**Highest phase reached**

Phase 3

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL4650437)

## Names and chemistry

**Drug type**

Antibody

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL4650437)

**Drug name**

Ebdarokimab

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL4650437)

### Other names (15)

- ak 101
- AK-101
- ak101
- Ak101
- AK101
- ak101 iv
- AK101 IV
- ebdarokimab
- Ebdarokimab
- ebdarokimab \[INN\]
- Ebdarokimab \[WHO-DD\]
- ebdarokimab inn
- ebdarokimab who dd
- immunoglobulin g1 anti human interleukin 12 subunit beta human monoclonal ak101 gamma 1 chain disulfide with human monoclonal ak101 kappa chain dimer
- IMMUNOGLOBULIN G1, ANTI-(HUMAN INTERLEUKIN 12 SUBUNIT .BETA.) (HUMAN MONOCLONAL AK101 .GAMMA.1-CHAIN), DISULFIDE WITH HUMAN MONOCLONAL AK101 .KAPPA.-CHAIN, DIMER

## Identifiers

**CAS registry numbers**

- 2393651-11-9

**ChEMBL ID**

CHEMBL4650437

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL4650437)

**FDA ingredient codes (UNII)**

- PG97J3111A

## Regulatory information

### Other regulatory facts

**First in class**

No

**Orphan designation**

No

## Pharmacology

### Drug classification

**Pharmacology name**

ebdarokimab

**Type**

Antibody

**Drug name stem**

\-mab

**Approval recorded by Guide to Pharmacology**

Yes

### Mechanisms of action (5)

- **Action**  
Binding

**Action type**  
Binding

**Target**  
IL-12B

**Gene symbol**  
IL-12B
- **Mechanism**  
Interleukin-12 inhibitor

**Action type**  
Inhibitor

**Target**  
Interleukin-12

**Protein identifier**  
P29459
- **Mechanism**  
Interleukin-12 inhibitor

**Action type**  
Inhibitor

**Target**  
Interleukin-12

**Protein identifier**  
P29460
- **Mechanism**  
Interleukin-23 inhibitor

**Action type**  
Inhibitor

**Target**  
Interleukin-23

**Protein identifier**  
P29460
- **Mechanism**  
Interleukin-23 inhibitor

**Action type**  
Inhibitor

**Target**  
Interleukin-23

**Protein identifier**  
Q9NPF7

### Open Targets mechanisms (2)

- **Mechanism**  
Interleukin-12 inhibitor

**Action type**  
Inhibitor

**Target**  
Interleukin-12
- **Mechanism**  
Interleukin-23 inhibitor

**Action type**  
Inhibitor

**Target**  
Interleukin-23

### Investigated indications (3)

- **Condition**  
Psoriasis

**Highest recorded phase**  
3

**Condition identifier**  
EFO:0000676

**Subject identifier**  
D011565
- **Condition**  
Colitis, Ulcerative

**Highest recorded phase**  
1

**Condition identifier**  
EFO:0000729

**Subject identifier**  
D003093
- **Condition**  
Psoriasis

**Highest recorded phase**  
3

**Condition identifier**  
EFO:1001494

**Subject identifier**  
D011565

### Open Targets indications (5)

- **Condition identifier**  
EFO\_0000676

**Highest recorded phase**  
2
- **Condition identifier**  
EFO\_0000729

**Highest recorded phase**  
1
- **Condition identifier**  
EFO\_1001494

**Highest recorded phase**  
3
- **Condition identifier**  
MONDO\_0005083

**Highest recorded phase**  
2
- **Condition identifier**  
MONDO\_0005101

**Highest recorded phase**  
1

### Trial references (5)

- NCT04172233  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT04172233)
- NCT04173637  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT04173637)
- NCT05120297  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05120297)
- NCT05509361  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05509361)
- NCT06281704  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06281704)

## Chemical properties

**Prodrug**

No

**Chirality**

Single enantiomer

**Inorganic**

No

**Natural product**

No

## Related records

### Trials (5)

- A Clinical Study of AK101 in Subjects With Moderate to Severe Plaque Psoriasis
- A Phase 3 Study of Efficacy and Safety of AK101 in Subjects With Psoriasis
- A Study of AK101 in Subjects With Moderately to Severely Active Ulcerative Colitis
- Clinical Study of AK101 in Subjects With Moderate to Severe Plaque Psoriasis
- [Open Label Study to Evaluate the Safety and Efficacy of AK101 Injection Subcutaneously in Subjects With Psoriasis](https://trialight.com/data/trial/open-label-study-to-evaluate-the-safety-and-efficacy-of-e9a1ae53-b554-42d5-9095-4e156681a5b9.md)

### In development for (3)

- Palmoplantar pustulosis Phase 3
- [Psoriasis](https://trialight.com/data/condition/psoriasis-4340caf0-883c-54c7-886d-31e59b80dead.md) Phase 3
- [Ulcerative colitis](https://trialight.com/data/condition/ulcerative-colitis-afbc4579-f001-5a8a-b904-28f09f344ab5.md) Phase 1

### Targets (3)

- [IL12A](https://trialight.com/data/target/il12a-f7e63dfd-cd53-5ed7-ab6b-30bc302a7278.md) Interleukin-12 inhibitor
- [IL12B](https://trialight.com/data/target/il12b-92e53178-7b56-555c-ac6b-a1235d8fe7e5.md) Interleukin-12 inhibitor
- [IL23A](https://trialight.com/data/target/il23a-e11f3992-27b4-5bef-9242-07ab6ac420e9.md) Interleukin-23 inhibitor

---

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