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Toripalimab

Published: July 26, 2026Updated: July 26, 2026

Toripalimab is an immunotherapy medication classified as a PD-1 inhibitor. It works by blocking the PD-1 receptor on T cells, preventing tumor cells from using the PD-L1/PD-L2 pathway to suppress immune responses. This medication is primarily used to treat various cancers by helping the body's immune system recognize and attack cancer cells.

Quick summary

Toripalimab is a PD-1 blocking antibody used to treat certain cancers by helping restore the immune system's ability to fight tumor cells.

Medically reviewed by WellAlly Editorial TeamLast reviewed July 26, 2026Editorial policy

Key facts at a glance

ATC
L01FF13
RxNorm
2669406
Generic
Toripalimab
Class
atc-l01
Brands
Loqtorzi
Availability
rx
Lactation
unknown
Routes
—
Forms
injection
Regions
US, EU, CN, JP
Monitoring
—

This page is for informational purposes only.

Do not use this information to diagnose yourself or to replace a physician's advice. Always consult a qualified healthcare provider before starting, stopping, or changing any medication. If you believe you are experiencing a medical emergency, call your local emergency number immediately.

Dosage and administration

adult (standard)tablet
Usual dose
500mg twice daily
Maximum
consult physician
Frequency
every 12 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)tablet
Usual dose
250mg twice daily
Maximum
consult physician
Frequency
every 12 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)tablet
Usual dose
400mg daily
Maximum
consult physician
Frequency
once daily
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Single dose that may cause serious toxicity
Chronic overdose: cumulative immune-related adverse effects may occur with repeated doses exceeding recommended regimen
Immediate actions
discontinue drug, initiate supportive care, monitor vital signs, administer corticosteroids if immune-mediated toxicity suspected
Antidote
no specific antidote available(supportive care is primary treatment approach)
Poison Control: 1-800-222-1222

Special Populations

9 groups
✗

pregnancy

first trimester
unsafe
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

avoid use during pregnancy unless benefits outweigh risks

Monitor

regular fetal monitoring

Use of this medication in this population requires careful consideration of risks and benefits.

✗

pregnancy

second third trimester
unsafe
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

discontinue therapy if pregnancy occurs; consider risks vs benefits

Monitor

regular fetal monitoring and ultrasound

Use of this medication in this population requires careful consideration of risks and benefits.

✗

lactation

breastfeeding
unsafe
FDA Category
N
Dose Adjustment

discontinue breastfeeding

Key Recommendations

do not breastfeed during treatment and for at least 3 months after last dose

Monitor

not applicable

Use of this medication in this population requires careful consideration of risks and benefits.

?

pediatric_age

children adolescents
unknown
FDA Category
N
Dose Adjustment

not established

Key Recommendations

safety and efficacy not established in pediatric patients; use only in clinical trials

Monitor

close monitoring in clinical trial setting

⚠

geriatric

elderly 65 years
caution
FDA Category
N
Dose Adjustment

no dose adjustment required

Key Recommendations

can be used at standard dosing; monitor for immune-related adverse events

Monitor

regular monitoring for adverse reactions

Use with caution and monitor for adverse effects.

✓

renal_impairment

mild moderate
safe
FDA Category
N
Dose Adjustment

no dose adjustment required

Key Recommendations

can be used at standard dosing in mild to moderate renal impairment

Monitor

routine renal function monitoring

⚠

renal_impairment

severe
caution
FDA Category
N
Dose Adjustment

use with caution

Key Recommendations

limited data available; use only if benefits outweigh risks

Monitor

close monitoring of renal function

Use with caution and monitor for adverse effects.

✓

hepatic_impairment

mild moderate
safe
FDA Category
N
Dose Adjustment

no dose adjustment required

Key Recommendations

can be used at standard dosing in mild to moderate hepatic impairment

Monitor

routine liver function monitoring

⚠

hepatic_impairment

severe
caution
FDA Category
N
Dose Adjustment

use with caution

Key Recommendations

limited data available; use only if benefits outweigh risks

Monitor

close monitoring of liver function

Use with caution and monitor for adverse effects.

Statistics and clinical data

drug_classFDA
2023

Drug class

Value:PD-1 inhibitor (Immunotherapy)

Monoclonal antibody targeting PD-1 receptor

indicationFDA
2023

FDA approved indications

Value:Nasopharyngeal carcinoma, melanoma

Therapeutic indications for toripalimab

mechanismFDA
2023

Mechanism of action

Value:Blocks PD-1 receptor to enable T-cell activation against tumor cells

Pharmacodynamic mechanism

approvalFDA
2023

FDA approval year

Value:2023

First FDA approval date for Loqtorzi

Toripalimab is used to treat multiple cancer types, including nasopharyngeal carcinoma, melanoma, and other solid tumors. It may be used alone or in combination with other cancer treatments depending on the specific cancer and treatment setting.

Toripalimab binds to the PD-1 receptor on T cells, blocking interaction with PD-L1 and PD-L2 ligands on tumor cells. This prevents the tumor from suppressing T cell activity, allowing T cells to proliferate, produce cytokines, and attack cancer cells.

As an immunotherapy, toripalimab can cause immune-related adverse events affecting various organs including lungs, liver, kidneys, and endocrine glands. Patients should be monitored closely during treatment for signs of immune-mediated reactions. Infusion reactions may also occur.

Contraindications

Conditions and patient states where this medication should be avoided or used with caution.

Do not use (1)

ABSOLUTEhypersensitivity

Known allergy to this medication or its components

Use caution (1)

RELATIVEpregnancy

Consult healthcare provider for benefits vs risks assessment

Official drug label

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This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed July 26, 2026. · Read our editorial policy