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chemotherapy(c-ATT)
chemotherapy(c-ATT) is a Topoisomerase inhibitor Small molecule drug developed by Sun Yat-sen University. It is currently in Phase 3 development for Treatment of various cancers. Also known as: c-ATT.
C-ATT works by targeting and inhibiting the function of cancer cells.
Chemotherapy, specifically the CHOP regimen, is used to treat high-risk, previously untreated adults with T-cell Lymphoma. The CHOP regimen typically involves a combination of bleomycin sulfate and cisplatin, along with other medications, to target and eliminate cancer cells.
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Baseline phase 3 → approval rate
+58.3pp
Industry-wide phase 3 drugs reach approval ~58.3% of the time (BIO/Informa 2023 industry benchmark across all therapeutic areas). -
Oncology Phase 3 boost
+3.0pp
Oncology Phase 3 trials have higher approval rates (~61%) than the cross-industry average due to clearer endpoints and FDA oncology pathway.
| Regulator | Country | Likely year | Lag vs FDA |
|---|---|---|---|
| FDA | US | 2028–2030 | — |
| EMA | EU | 2029–2031 | +0.7 yr |
| MHRA | GB | 2029–2031 | +0.7 yr |
| Health Canada | CA | 2029–2032 | +0.9 yr |
| TGA | AU | 2029–2032 | +1.2 yr |
| PMDA | JP | 2029–2032 | +1.5 yr |
| NMPA | CN | 2030–2033 | +2.3 yr |
| MFDS | KR | 2029–2032 | +1.4 yr |
| CDSCO | IN | 2029–2033 | +1.8 yr |
| ANVISA | BR | 2030–2033 | +2.3 yr |
Hover any row for the lag rationale. Lag estimates are reduced when the drug has FDA Breakthrough or EMA PRIME designation (sponsors file globally in parallel).
Estimate based on the BIO/Informa industry phase transition rates plus per-drug modifiers for therapeutic area, sponsor type, FDA designations, mechanism, and trial design. Per-jurisdiction lags from Tufts CSDD international approval studies. Not investment, clinical or regulatory advice. Methodology: /methodology#likelihood.
At a glance
| Generic name | chemotherapy(c-ATT) |
|---|---|
| Also known as | c-ATT |
| Sponsor | Sun Yat-sen University |
| Drug class | Topoisomerase inhibitor |
| Target | Topoisomerase II |
| Modality | Small molecule |
| Therapeutic area | Oncology |
| Phase | Phase 3 |
Mechanism of action
C-ATT is a chemotherapy drug that interferes with the DNA replication process in cancer cells, ultimately leading to cell death. This is achieved through the inhibition of topoisomerase II, an enzyme essential for DNA replication. As a result, cancer cells are unable to divide and grow, leading to tumor shrinkage and reduced cancer progression.
Approved indications
- Treatment of various cancers
Common side effects
- Myelosuppression
- Nausea and vomiting
- Hair loss
- Fatigue
Key clinical trials
- Combination Chemotherapy in Treating Patients With Intermediate-Grade or Immunoblastic Non-Hodgkin's Lymphoma (PHASE3)
- A Study of Improving the Efficacy of Treatment in High Risk T Cell Lymphoma Patients (PHASE3)
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:
- chemotherapy(c-ATT) CI brief — competitive landscape report
- chemotherapy(c-ATT) updates RSS · CI watch RSS
- Sun Yat-sen University portfolio CI
Frequently asked questions about chemotherapy(c-ATT)
What is chemotherapy(c-ATT)?
How does chemotherapy(c-ATT) work?
What is chemotherapy(c-ATT) used for?
Who makes chemotherapy(c-ATT)?
Is chemotherapy(c-ATT) also known as anything else?
What drug class is chemotherapy(c-ATT) in?
What development phase is chemotherapy(c-ATT) in?
What are the side effects of chemotherapy(c-ATT)?
What does chemotherapy(c-ATT) target?
Related
- Drug class: All Topoisomerase inhibitor drugs
- Target: All drugs targeting Topoisomerase II
- Manufacturer: Sun Yat-sen University — full pipeline
- Therapeutic area: All drugs in Oncology
- Indication: Drugs for Treatment of various cancers
- Also known as: c-ATT
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing