> Trialight public data. Index of pages: https://trialight.com/llms.txt
> Web page: https://trialight.com/data/asset/tremelimumab-24e58585-33c8-4837-b098-dae8de9e4d79
> Record changed: 2026-10-13

# Tremelimumab

Highest phase reached

Approved

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL2108658)

Drug type

Antibody

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL2108658)

First approval year

2022

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL2108658)

## Development status

**First approval year**

2022

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL2108658)

**Listing at source**

Listed

**Highest phase reached**

Approved

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL2108658)

## Names and chemistry

**Drug type**

Antibody

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL2108658)

**Drug name**

Tremelimumab

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL2108658)

### Brand names (4)

- imjudo
- Imjudo
- tremelimumab astrazeneca
- Tremelimumab astrazeneca

### Other names (37)

- cp 675 206
- cp 675206
- CP-675,206
- CP-675206
- durvalumab medi4736 and tremelimumab
- durvalumab tremelimumab
- immunoglobulin g2 anti human ctla 4 antigen human monoclonal cp 675206 clone 11 2 1 heavy chain disulfide with human monoclonal cp 675206 clone 11 2 1 light chain dimer
- immunoglobulin g2 anti human ctla 4 antigen human monoclonal cp 675206 clone 11 2 1 heavy chain disulphide with human monoclonal cp 675206 clone 11 2 1 light chain dimer
- IMMUNOGLOBULIN G2, ANTI-(HUMAN CTLA-4 (ANTIGEN)) (HUMAN MONOCLONAL CP-675206 CLONE 11.2.1 HEAVY CHAIN) DISULFIDE WITH HUMAN MONOCLONAL CP-675206 CLONE 11.2.1 LIGHT CHAIN, DIMER
- IMMUNOGLOBULIN G2, ANTI-(HUMAN CTLA-4 (ANTIGEN)) (HUMAN MONOCLONAL CP-675206 CLONE 11.2.1 HEAVY CHAIN) DISULPHIDE WITH HUMAN MONOCLONAL CP-675206 CLONE 11.2.1 LIGHT CHAIN, DIMER
- pf 06753388
- PF-06753388
- ticilimumab
- TICILIMUMAB
- tremelimumab
- Tremelimumab
- Tremelimumab (genetical recombination)
- TREMELIMUMAB (GENETICAL RECOMBINATION) \[JAN\]
- tremelimumab (treme)
- tremelimumab \[INN\]
- TREMELIMUMAB \[JAN\]
- Tremelimumab \[MI\]
- TREMELIMUMAB \[USAN\]
- Tremelimumab \[WHO-DD\]
- tremelimumab actl

And 12 more, listed on the interactive page.

## Identifiers

**ATC classification codes**

- L01FX20

Sources for recorded values

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL2108658)

**CAS registry numbers**

- 745013-59-6

**ChEMBL ID**

CHEMBL2108658

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL2108658)

**FDA ingredient codes (UNII)**

- QEN1X95CIX

### RxNorm IDs (RxCUI) (2)

- 2619312
- 2619313

## Regulatory information

### United States

**Applicant**

ASTRAZENECA AB

**Approval date**

21 Oct 2022

**Application number**

BLA761289

### European Union

**Status**

Authorised

**Status date**

20 Feb 2023

**Authorisation date**

20 Feb 2023

**Approved indications**

Imjudo in combination with durvalumab is indicated for the first line treatment of adults with advanced or unresectable hepatocellular carcinoma (HCC). Imjudo in combination with durvalumab and platinum-based chemotherapy is indicated for the first-line treatment of adults with metastatic non-small cell lung cancer (NSCLC) with no sensitising EGFR mutations or ALK positive mutations.

**Product number**

EMEA/H/C/006016

**Authorisation holder**

AstraZeneca AB

**Priority medicines scheme**

No

**Generic**

No

**Biosimilar**

No

**Generic medicines**

0

**Biosimilar medicines**

0

**Advanced therapy**

No

**Conditional approval**

No

**Additional monitoring**

Yes

**Accelerated assessment**

No

**Exceptional circumstances**

No

#### Therapeutic areas

- Carcinoma, Hepatocellular
- Carcinoma, Non-Small-Cell Lung

European medicines record

Source: [www.ema.europa.eu](https://www.ema.europa.eu/en/medicines/human/EPAR/imjudo)

### Other regulatory facts

**Patents**

0

**Designations**

2

**Earliest recorded loss of exclusivity**

21 Oct 2029

**First in class**

No

**Fast track**

No

**Breakthrough designation**

No

**Orphan designation**

No

**Priority review**

No

**Orphan exclusivity**

No

**Accelerated approval**

No

**Availability**

Prescription only

## Pharmacology

### Drug classification

**Pharmacology name**

tremelimumab

**Type**

Antibody

**Drug name stem**

\-mab

**Approval recorded by Guide to Pharmacology**

Yes

#### Administration routes

- Parenteral

### Mechanisms of action (2)

- **Action**  
Binding

**Action type**  
Binding

**Target**  
cytotoxic T-lymphocyte-associated protein 4 (CD152)

**Gene symbol**  
CTLA4

**Protein identifier**  
P16410

**Median affinity**

8.91

**Affinity units**  
pKd

**Primary target**  
Yes
- **Mechanism**  
Cytotoxic T-lymphocyte protein 4 inhibitor

**Action type**  
Inhibitor

**Target**  
Cytotoxic T-lymphocyte protein 4

**Protein identifier**  
P16410

### Open Targets mechanisms

- **Mechanism**  
Cytotoxic T-lymphocyte protein 4 inhibitor

**Action type**  
Inhibitor

**Target**  
Cytotoxic T-lymphocyte protein 4

### Investigated indications (61)

- **Condition**  
Carcinoma, Squamous Cell

**Highest recorded phase**  
3

**Condition identifier**  
EFO:0000181

**Subject identifier**  
D002294
- **Condition**  
Carcinoma, Hepatocellular

**Highest recorded phase**  
4

**Condition identifier**  
EFO:0000182

**Subject identifier**  
D006528
- **Condition**  
Myelodysplastic Syndromes

**Highest recorded phase**  
1

**Condition identifier**  
EFO:0000198

**Subject identifier**  
D009190
- **Condition**  
Squamous Cell Carcinoma of Head and Neck

**Highest recorded phase**  
2

**Condition identifier**  
EFO:0000199

**Subject identifier**  
D000077195
- **Condition**  
Breast Neoplasms

**Highest recorded phase**  
2

**Condition identifier**  
EFO:0000305

**Subject identifier**  
D001943
- **Condition**  
Carcinoma, Renal Cell

**Highest recorded phase**  
3

**Condition identifier**  
EFO:0000349

**Subject identifier**  
D002292
- **Condition**  
Colorectal Neoplasms

**Highest recorded phase**  
2

**Condition identifier**  
EFO:0000365

**Subject identifier**  
D015179
- **Condition**  
Melanoma

**Highest recorded phase**  
3

**Condition identifier**  
EFO:0000389

**Subject identifier**  
D008545
- **Condition**  
Lymphoma, Large B-Cell, Diffuse

**Highest recorded phase**  
1

**Condition identifier**  
EFO:0000403

**Subject identifier**  
D016403
- **Condition**  
Adenocarcinoma, Follicular

**Highest recorded phase**  
2

**Condition identifier**  
EFO:0000501

**Subject identifier**  
D018263
- **Condition**  
Stomach Neoplasms

**Highest recorded phase**  
2

**Condition identifier**  
EFO:0000503

**Subject identifier**  
D013274
- **Condition**  
Neoplasms, Germ Cell and Embryonal

**Highest recorded phase**  
2

**Condition identifier**  
EFO:0000514

**Subject identifier**  
D009373
- **Condition**  
Glioblastoma

**Highest recorded phase**  
2

**Condition identifier**  
EFO:0000519

**Subject identifier**  
D005909
- **Condition**  
Lymphoma

**Highest recorded phase**  
1

**Condition identifier**  
EFO:0000574

**Subject identifier**  
D008223
- **Condition**  
Mesothelioma

**Highest recorded phase**  
2

**Condition identifier**  
EFO:0000588

**Subject identifier**  
D008654
- **Condition**  
Neoplasms

**Highest recorded phase**  
4

**Condition identifier**  
EFO:0000616

**Subject identifier**  
D009369
- **Condition**  
Thyroid Neoplasms

**Highest recorded phase**  
2

**Condition identifier**  
EFO:0000641

**Subject identifier**  
D013964
- **Condition**  
Prostatic Neoplasms

**Highest recorded phase**  
2

**Condition identifier**  
EFO:0000673

**Subject identifier**  
D011471
- **Condition**  
Carcinoma, Renal Cell

**Highest recorded phase**  
3

**Condition identifier**  
EFO:0000681

**Subject identifier**  
D002292
- **Condition**  
Sarcoma

**Highest recorded phase**  
2

**Condition identifier**  
EFO:0000691

**Subject identifier**  
D012509
- **Condition**  
Small Cell Lung Carcinoma

**Highest recorded phase**  
3

**Condition identifier**  
EFO:0000702

**Subject identifier**  
D055752
- **Condition**  
Carcinoma, Squamous Cell

**Highest recorded phase**  
3

**Condition identifier**  
EFO:0000708

**Subject identifier**  
D002294
- **Condition**  
Melanoma

**Highest recorded phase**  
3

**Condition identifier**  
EFO:0000756

**Subject identifier**  
D008545
- **Condition**  
HIV Infections

**Highest recorded phase**  
2

**Condition identifier**  
EFO:0000764

**Subject identifier**  
D015658
- **Condition**  
Ovarian Neoplasms

**Highest recorded phase**  
2

**Condition identifier**  
EFO:0001075

**Subject identifier**  
D010051

And 36 more, listed on the interactive page.

### Open Targets indications (124)

- **Condition identifier**  
EFO\_0000181

**Highest recorded phase**  
3
- **Condition identifier**  
EFO\_0000182
- **Condition identifier**  
EFO\_0000199
- **Condition identifier**  
EFO\_0000389

**Highest recorded phase**  
2
- **Condition identifier**  
EFO\_0000503

**Highest recorded phase**  
2
- **Condition identifier**  
EFO\_0000514

**Highest recorded phase**  
2
- **Condition identifier**  
EFO\_0000588

**Highest recorded phase**  
2
- **Condition identifier**  
EFO\_0000616
- **Condition identifier**  
EFO\_0000673

**Highest recorded phase**  
2
- **Condition identifier**  
EFO\_0000681

**Highest recorded phase**  
3
- **Condition identifier**  
EFO\_0000691

**Highest recorded phase**  
2
- **Condition identifier**  
EFO\_0000702

**Highest recorded phase**  
3
- **Condition identifier**  
EFO\_0000708

**Highest recorded phase**  
2
- **Condition identifier**  
EFO\_0000756

**Highest recorded phase**  
3
- **Condition identifier**  
EFO\_0000764

**Highest recorded phase**  
2
- **Condition identifier**  
EFO\_0002618

**Highest recorded phase**  
2
- **Condition identifier**  
EFO\_0003060
- **Condition identifier**  
EFO\_0003860
- **Condition identifier**  
EFO\_0003863

**Highest recorded phase**  
3
- **Condition identifier**  
EFO\_0003891

**Highest recorded phase**  
2
- **Condition identifier**  
EFO\_0004142

**Highest recorded phase**  
2
- **Condition identifier**  
EFO\_0008528

**Highest recorded phase**  
2
- **Condition identifier**  
EFO\_1000355

**Highest recorded phase**  
3
- **Condition identifier**  
EFO\_1000616

**Highest recorded phase**  
2
- **Condition identifier**  
EFO\_1001331

**Highest recorded phase**  
2

And 99 more, listed on the interactive page.

### Reported adverse events (49)

- **Event**  
adrenal insufficiency

**Reports**  
12

**Reporting signal score**

21.3427
- **Event**  
appendicitis

**Reports**  
9

**Reporting signal score**

15.7876
- **Event**  
asthenia

**Reports**  
4

**Reporting signal score**

8.45602
- **Event**  
autoimmune hepatitis

**Reports**  
12

**Reporting signal score**

25.271
- **Event**  
autoimmune nephritis

**Reports**  
6

**Reporting signal score**

28.0924
- **Event**  
autoimmune pancreatitis

**Reports**  
5

**Reporting signal score**

19.4324
- **Event**  
bacillus infection

**Reports**  
3

**Reporting signal score**

10.3677
- **Event**  
bile duct stenosis

**Reports**  
15

**Reporting signal score**

61.0911
- **Event**  
biliary tract infection

**Reports**  
35

**Reporting signal score**

203.104
- **Event**  
cauda equina syndrome

**Reports**  
3

**Reporting signal score**

8.68181
- **Event**  
cholangitis infective

**Reports**  
3

**Reporting signal score**

12.6104
- **Event**  
colitis

**Reports**  
54

**Reporting signal score**

118.935
- **Event**  
dizziness

**Reports**  
3

**Reporting signal score**

15.6638
- **Event**  
drug-induced liver injury

**Reports**  
17

**Reporting signal score**

20.2001
- **Event**  
embolism

**Reports**  
12

**Reporting signal score**

25.2596
- **Event**  
endocrine disorder

**Reports**  
3

**Reporting signal score**

8.72653
- **Event**  
endocrine toxicity

**Reports**  
2

**Reporting signal score**

10.9964
- **Event**  
enterocolitis

**Reports**  
7

**Reporting signal score**

13.052
- **Event**  
enterocolitis infectious

**Reports**  
9

**Reporting signal score**

33.8381
- **Event**  
febrile neutropenia

**Reports**  
27

**Reporting signal score**

24.2461
- **Event**  
gallbladder obstruction

**Reports**  
3

**Reporting signal score**

13.3802
- **Event**  
headache

**Reports**  
5

**Reporting signal score**

15.8908
- **Event**  
hepatic function abnormal

**Reports**  
14

**Reporting signal score**

11.688
- **Event**  
hepatic infection

**Reports**  
11

**Reporting signal score**

48.9033
- **Event**  
hepatitis

**Reports**  
14

**Reporting signal score**

14.7353

And 24 more, listed on the interactive page.

### Trial references (162)

- NCT00086489  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT00086489)
- NCT00254579  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT00254579)
- NCT00257205  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT00257205)
- NCT00431275  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT00431275)
- NCT00585000  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT00585000)
- NCT01103635  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT01103635)
- NCT02535078  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT02535078)
- NCT04223648  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT04223648)
- NCT00312975  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT00312975)
- NCT02000947  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT02000947)
- NCT02040064  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT02040064)
- NCT02179671  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT02179671)
- NCT02352948  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT02352948)
- NCT02453282  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT02453282)
- NCT02542293  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT02542293)
- NCT03130764  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT03130764)
- NCT03164616  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT03164616)
- NCT03164772  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT03164772)
- NCT03237377  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT03237377)
- NCT03275597  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT03275597)
- NCT03319316  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT03319316)
- NCT03581487  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT03581487)
- NCT03965468  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT03965468)
- NCT03975114  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT03975114)
- NCT03994393  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT03994393)

And 137 more, listed on the interactive page.

## Dosing

**Dose**

75 mg

**Route**

Intravenous

**How often**

Every 3 weeks

### Conditions of use

- Administer over 60 minutes after dilution

## Chemical properties

**Prodrug**

No

**Chirality**

Single enantiomer

**Inorganic**

No

**Natural product**

No

## National Drug Codes

- 0310-4505
- 0310-4535

## Related records

### Trials (249)

- ......SMARTEST Trial......
- A Clinical Study With Tremelimumab as Monotherapy in Malignant Mesothelioma
- A Clinical Trial of Durvalumab and Tremelimumab, Administered With Radiation Therapy or Ablation in Patients With Colorectal Cancer
- A Global Study to Assess the Effects of MEDI4736 (Durvalumab), Given as Monotherapy or in Combination With Tremelimumab Determined by PD-L1 Expression Versus Standard of Care in Patients With Locally Advanced or Metastatic Non Small Cell Lung Cancer
- A Phase 1 Study of MEDI4736 in Combination With Tremelimumab in Subjects With Advanced Solid Tumors
- A Phase 1 Study Testing CP-675,206 In Combination With Gemcitabine In Patients With Previously Untreated, Advanced Pancreatic Cancer
- A Phase 1 Study To Evaluate Escalating Doses Of A Vaccine-Based Immunotherapy Regimen For Prostate Cancer (PrCa VBIR)
- A Phase 1 Study to Evaluate MEDI4736 in Combination With Tremelimumab
- A Phase 1/2 Study of Durvalumab(MEDI4736) and Tremelimumab in Chinese Patients With Advanced Malignancies
- A Phase 1b Study of MEDI4736 in Combination With Tremelimumab in Subjects With Advanced Non-small Cell Lung Cancer
- A Phase 1b/2 Safety and Tolerability Study of MEDI6469 in Combination With Therapeutic Immune Agents or Monoclonal Antibodies
- A Phase 1b/2 Study of MEDI4736 With Tremelimumab, MEDI4736 or Tremelimumab Monotherapy in Gastric or GEJ Adenocarcinoma
- A Phase 2 Study of Durvalumab in Combination With Tremelimumab in Malignant Pleural Mesothelioma
- A Phase I Dose Escalation and Dose Expansion Study to Investigate the Pharmacokinetics and Safety of Subcutaneous Durvalumab
- A Phase I Study to Evaluate the Safety, Tolerability and Efficacy of MEDI4736 (Durvalumab) With Tremelimumab in Head and Neck Cancer
- A Phase I, Open-Label, Multicentre Study to Evaluate the Safety, Tolerability and Pharmacokinetics of MEDI4736 in Patients With Advanced Solid Tumours
- A Phase I/II Study of Pexa-Vec Oncolytic Virus in Combination With Immune Checkpoint Inhibition in Refractory Colorectal Cancer
- A Phase II Study of Durvalumab Treatment - Substudy A: In Patients Who Discontinued Prior Checkpoint Therapy Due to Immune Related Toxicity - Substudy B: For Continued Treatment (+/- Tremelimumab) of Patients Previously Enrolled to Completed CCTG Studies
- A Phase II Study of Neoadjuvant Chemotherapy Plus Durvalumab (MEDI4736) and Tremelimumab in Advanced-stage Ovarian Cancer (TRU-D)
- A Phase II Study of Single Tremelimumab With Regular Interval Durvalumab Plus Gemcitabine and Cisplatin in Locally Advanced Unresectable/Metastatic Combined Hepatocellular-cholangiocarcinoma

### Approved for (4)

- [Cancer](https://trialight.com/data/condition/cancer-703b1dfc-4812-50eb-83f4-d7a205d16bdb.md)
- [Hepatocellular carcinoma](https://trialight.com/data/condition/hepatocellular-carcinoma-fc1014ac-5a3c-551d-98ea-95306009e299.md)
- Neoplasm
- [Non-small cell lung carcinoma](https://trialight.com/data/condition/non-small-cell-lung-carcinoma-a86c1d60-523f-5ea7-a5e1-39ed4a2296f8.md)

### In development for (58)

- Bile duct cancer Phase 2
- [Biliary tract cancer](https://trialight.com/data/condition/biliary-tract-cancer-6b9535c9-ccaa-5b47-8c46-0d05d39d7c62.md) Phase 2
- [Biliary tract neoplasm](https://trialight.com/data/condition/biliary-tract-neoplasm-5b757066-5940-52f7-aa7d-e5aafdc5b54e.md) Phase 2
- [Breast cancer](https://trialight.com/data/condition/breast-cancer-8ac10da3-93bd-54c5-a93b-265bc6699689.md) Phase 2
- Breast carcinoma Phase 2
- [Cholangiocarcinoma](https://trialight.com/data/condition/cholangiocarcinoma-3777afe4-5189-5eb1-82f8-0c3446cb902f.md) Phase 2
- [Clear cell renal carcinoma](https://trialight.com/data/condition/clear-cell-renal-carcinoma-789eee25-ec64-5771-9b7d-d19544781b11.md) Phase 3
- [Colorectal adenocarcinoma](https://trialight.com/data/condition/colorectal-adenocarcinoma-49107d5a-ece1-5f2b-8783-f2077e298ffa.md) Phase 2
- [Colorectal cancer](https://trialight.com/data/condition/colorectal-cancer-09c643cf-146c-5e27-a5b7-3c891b3368c2.md) Phase 2
- [Colorectal neoplasm](https://trialight.com/data/condition/colorectal-neoplasm-31f0a633-3abe-5df4-9d3a-9292c6541f1d.md) Phase 2
- [Cutaneous melanoma](https://trialight.com/data/condition/cutaneous-melanoma-c6e75b71-1c7c-59fe-a087-174eb0ec53df.md) Phase 3
- [Diffuse large B-cell lymphoma](https://trialight.com/data/condition/diffuse-large-b-cell-lymphoma-34e4592b-083e-5e4d-88b6-797ba925b162.md) Phase 1
- Dysgerminoma Phase 2
- [Esophageal cancer](https://trialight.com/data/condition/esophageal-cancer-a3b5271c-e6d4-537b-8dfd-9391c60e2af2.md) Phase 1
- Exocrine pancreatic carcinoma Phase 2
- [Fallopian tube cancer](https://trialight.com/data/condition/fallopian-tube-cancer-b95d05ee-41d5-565a-87e1-041170b88760.md) Phase 2
- Fallopian tube carcinoma Phase 2
- [Female reproductive organ cancer](https://trialight.com/data/condition/female-reproductive-organ-cancer-1207d84e-931f-51b6-90d9-6b2135cdebbb.md) Phase 2
- [Gastric adenocarcinoma](https://trialight.com/data/condition/gastric-adenocarcinoma-6bb74a55-7ba6-53e3-a113-22296a84d6ae.md) Phase 2
- [Gastric cancer](https://trialight.com/data/condition/gastric-cancer-3c1e2785-2672-5b3e-afce-9335f684c159.md) Phase 2

### Targets (1)

- [CTLA4](https://trialight.com/data/target/ctla4-ba502748-1564-5251-a6a1-96e2f7035fe9.md) Cytotoxic T-lymphocyte protein 4 inhibitor

---

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