> Trialight public data. Index of pages: https://trialight.com/llms.txt
> Web page: https://trialight.com/data/asset/azirkitug-4abb572a-80a6-453e-816e-6de029b59181
> Record changed: 2026-10-13

# Azirkitug

Highest phase reached

Phase 2

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL6068092)

Drug type

Protein

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL6068092)

## Development status

**Listing at source**

Listed

**Highest phase reached**

Phase 2

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL6068092)

## Names and chemistry

**Drug type**

Protein

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL6068092)

**Drug name**

Azirkitug

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL6068092)

### Other names (16)

- azirkitug
- Azirkitug
- azirkitug \[INN\]
- AZIRKITUG \[USAN\]
- azirkitug inn
- azirkitug usan
- h gamma1 heavy chain humanized 1 450 vh homo sapiens ighv3 73 01 84 8 ighd ighj4 01 92 9 cdr imgt 8 10 11 26 33 51 60 99 109 1 120 homo sapiens ighg1 03v g1m3 g1m17 ng1m1 ch1 k120 ch3 e12 m14 ch1 r120 k 217 121 218 hinge 1 15 219 233 ch2 234 343 ch3 e12 359 m14 361 344 448 chs 449 450 121 450 223 214 disulfide with l kappa light chain humanized 1 214 v kappa homo sapiens igkv3 11 01 78 9 igkj2 01 100 cdr imgt 6 3 9 27 32 50 52 89 97 1 107 homo sapiens igkc 01 100 km3 a45 1 153 v101 191 108 214 dimer 229 229 232 232 bisdisulfide produced in a chinese hamster ovary cho cell line derived from the cell line cho dux b11 lacking the enzyme dihydrofolate reductase dhfr and co expressing the rmd enzyme gdp 6 deoxy dlyxo 4 hexulose reductase glycoform alfa
- H-gamma1 heavy chain humanized (1-450) \[VH (Homo sapiens IGHV3-73\*01 (84.8%) -(IGHD) -IGHJ4\*01 (92.9%), CDR-IMGT\[8.10.11\] (26-33.51-60.99-109)) (1-120) -Homo sapiens IGHG1\*03v, G1m3>G1m17, nG1m1 CH1 K120, CH3 E12, M14 (CH1 R120>K (217) (121-218), hinge 1-15 (219-233), CH2 (234-343), CH3 E12 (359), M14 (361) (344-448), CHS (449-450)) (121-450)\], (223-214')-disulfide with L-kappa light chain humanized (1'-214') \[V-KAPPA (Homo sapiens IGKV3-11\*01 (78.9%) -IGKJ2\*01 (100%), CDR-IMGT \[6.3.9\] (27'-32'.50'-52'.89'-97')) (1'-107') -Homo sapiens IGKC\*01 (100%), Km3 A45.1 (153'), V101 (191') (108'-214')\]; dimer (229-229'':232-232'')-bisdisulfide, produced in a Chinese hamster ovary (CHO) cell line, derived from the cell line CHO-DUX-B11, lacking the enzyme dihydrofolate reductase (DHFR), and co-expressing the RMD enzyme (GDP-6-deoxy-Dlyxo-4-hexulose reductase), glycoform alfa
- immunoglobulin g1 anti human cc chemokine receptor ccr8 human rattus norvegicus monoclonal pr 1925514 γ1 chain disulfide with human rattus norvegicus monoclonal pr 1925514 κ chain dimer
- immunoglobulin g1 kappa anti homo sapiens ccr8 c c motif chemokine receptor 8 ckr l1 cdw198 humanized monoclonal antibody
- immunoglobulin G1-kappa, anti-\[Homo sapiens CCR8 (C-C motif chemokine receptor 8, CKR-L1, CDw198)\], humanized monoclonal antibody
- Immunoglobulin G1, anti-(human CC chemokine receptor CCR8) (human-Rattus norvegicus monoclonal PR-1925514 γ1-chain), disulfide with human-Rattus norvegicus monoclonal PR-1925514 κ-chain, dimer
- pr 1925514
- PR-1925514
- pr1925514
- PR1925514

## Identifiers

**CAS registry numbers**

- 2837169-12-5

**ChEMBL ID**

CHEMBL6068092

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL6068092)

**FDA ingredient codes (UNII)**

- R6HJ7X69JZ

## Regulatory information

### Other regulatory facts

**First in class**

No

**Orphan designation**

No

## Pharmacology

### Investigated indications

- **Condition**  
Neoplasms

**Highest recorded phase**  
2

**Condition identifier**  
EFO:0000616

**Subject identifier**  
D009369

### Open Targets indications (4)

- **Condition identifier**  
EFO\_0000616
- **Condition identifier**  
MONDO\_0005070
- **Condition identifier**  
MONDO\_0005233

**Highest recorded phase**  
1
- **Condition identifier**  
MONDO\_0010150

**Highest recorded phase**  
1

## Chemical properties

**Prodrug**

No

**Chirality**

Single enantiomer

**Inorganic**

No

**Natural product**

No

### Sequences (4)

- **Component**  
Heavy chain

**Type**  
Protein

**Sequence**  
EVQLVESGGGLVQPGGSLKLSCAASGFIFSNAVMYWVRQASGKGLEWVARIKTKFNNYATYYADAVKGRFTISRDDSKNMVYLQMNSLKTEDTAVYYCTAGDRNKPFAYWGQGTLVTVSSASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSSGLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKKVEPKSCDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSHEDPEVKFNWYVDGVEVHNAKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK
- **Component**  
Disulfide bridges

**Sequence**  
22-98 $ 22''-98'' $ 23'-88' $ 23'''-88''' $ 134'-194' $ 134'''-194''' $ 147-203 $ 147''-203'' $ 223-214' $ 223''-214''' $ 229-229'' $ 232-232'' $ 264-324 $ 264''-324'' $ 370-428 $ 370''-428''
- **Component**  
Light chain

**Type**  
Protein

**Sequence**  
ETVVTQSPATLSLSPGERATLSCRASTSVITLLHWFQQKPGQAPRLLIHGASNLESRVPARFSGSGSGTDFTLTISSLEPEDFATYFCQQSWNDPYTFGQGTKLEIKRTVAAPSVFIFPPSDEQLKSGTASVVCLLNNFYPREAKVQWKVDNALQSGNSQESVTEQDSKDSTYSLSSTLTLSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC
- **Component**  
Glycosylation sites (N)

**Sequence**  
300 $ 300''

## Related records

### Trials (1)

- [Study to Assess Adverse Events and Pharmacokinetics in Adult Participants With Non-Small Cell Lung Cancer, Head and Neck Squamous Cell Carcinoma and Other Solid Tumors, Receiving Intravenous Infusion of Azirkitug Alone or in Combination(s) With Budigalimab, Bevacizumab, or Telisotuzumab Adizutecan](https://trialight.com/data/trial/study-to-assess-adverse-events-and-pharmacokinetics-in-adult-75ac0852-abf8-4cb9-b25e-7ac41ffa0876.md)

### In development for (1)

- Neoplasm Phase 2

---

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