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Short-term Sintilimab
Short-term Sintilimab is a PD-1 inhibitor Small molecule drug developed by Shanghai Jiao Tong University School of Medicine. It is currently FDA-approved for Hodgkin lymphoma, Non-small cell lung cancer, Gastric cancer.
Sintilimab is a monoclonal antibody that blocks PD-1 on immune cells, allowing them to recognize and attack cancer cells.
Sintilimab is an antibody that acts as a programmed cell death protein 1 antagonist. It is being studied in combination with taxane and carboplatin for neoadjuvant therapy in triple-negative breast cancer, as well as in rectal cancer, among other conditions.
At a glance
| Generic name | Short-term Sintilimab |
|---|---|
| Sponsor | Shanghai Jiao Tong University School of Medicine |
| Drug class | PD-1 inhibitor |
| Target | PD-1 |
| Modality | Small molecule |
| Therapeutic area | Oncology |
| Phase | FDA-approved |
Mechanism of action
Sintilimab binds to programmed death receptor 1 (PD-1) on T cells, preventing interaction with PD-L1 and PD-L2 ligands expressed by tumor cells and immune cells. This blockade restores anti-tumor immune responses by reactivating exhausted T cells. The drug is used in short-term treatment regimens for various malignancies.
Approved indications
- Hodgkin lymphoma
- Non-small cell lung cancer
- Gastric cancer
- Esophageal squamous cell carcinoma
Common side effects
- Fatigue
- Decreased appetite
- Nausea
- Immune-related adverse events (pneumonitis, hepatitis, colitis)
- Infusion-related reactions
Key clinical trials
- Clinical Study on the Safety and Relationship of Sintilimab Combined With Chemotherapy in Neoadjuvant Treatment of Locally Advanced Rectal Adenocarcinoma (PHASE2)
- Short Course Radiotherapy With Sequential Disitamab Vedotin Combined With S-1 and Sintilimab as Whole Course Neoadjuvant Therapy for HER2 Expressed Locally Progressive Gastric Cancer (PHASE2)
- Short-term Sintilimab in Combination With Taxane and Carboplatin for Neoadjuvant Therapy in Triple-negative Breast Cancer (PHASE4)
- Sintilimab in Combination With Chidamide in Refractory and Relapsed ENKTCL (PHASE1, PHASE2)
- Sintilimab in Combination With Chidamide in Newly Diagnosed ENKTCL (PHASE2)
- Induction Chemotherapy Sequential Sintilimab Combined With Dual Epigenetic Drugs for ENKTL-HLH (PHASE2)
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |
Competitive intelligence
For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:
- Short-term Sintilimab CI brief — competitive landscape report
- Short-term Sintilimab updates RSS · CI watch RSS
- Shanghai Jiao Tong University School of Medicine portfolio CI
Frequently asked questions about Short-term Sintilimab
What is Short-term Sintilimab?
How does Short-term Sintilimab work?
What is Short-term Sintilimab used for?
Who makes Short-term Sintilimab?
What drug class is Short-term Sintilimab in?
What development phase is Short-term Sintilimab in?
What are the side effects of Short-term Sintilimab?
What does Short-term Sintilimab target?
Related
- Drug class: All PD-1 inhibitor drugs
- Target: All drugs targeting PD-1
- Manufacturer: Shanghai Jiao Tong University School of Medicine — full pipeline
- Therapeutic area: All drugs in Oncology
- Indication: Drugs for Hodgkin lymphoma
- Indication: Drugs for Non-small cell lung cancer
- Indication: Drugs for Gastric cancer
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing