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PAx5/PCMx5
PAx5/PCMx5 is a Multi-agent chemotherapy regimen Small molecule drug developed by SWOG Cancer Research Network. It is currently in Phase 3 development for Hematologic malignancies (specific indication dependent on SWOG trial protocol). Also known as: Lansoprazole: Prevacid.
PAx5/PCMx5 is a chemotherapy regimen combining prednisone, doxorubicin, cyclophosphamide, and other agents designed to treat hematologic malignancies.
PAx5/PCMx5 is a chemotherapy regimen combining prednisone, doxorubicin, cyclophosphamide, and other agents designed to treat hematologic malignancies. Used for Hematologic malignancies (specific indication dependent on SWOG trial protocol).
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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 | PAx5/PCMx5 |
|---|---|
| Also known as | Lansoprazole: Prevacid |
| Sponsor | SWOG Cancer Research Network |
| Drug class | Multi-agent chemotherapy regimen |
| Modality | Small molecule |
| Therapeutic area | Oncology |
| Phase | Phase 3 |
Mechanism of action
This is a multi-agent chemotherapy combination protocol used in cancer treatment. The exact composition and mechanism depend on the specific SWOG trial design, but typically involves cytotoxic agents that work through DNA damage and cell cycle disruption. PAx5/PCMx5 represents a standardized treatment regimen evaluated in phase 3 clinical trials.
Approved indications
- Hematologic malignancies (specific indication dependent on SWOG trial protocol)
Common side effects
- Myelosuppression
- Nausea and vomiting
- Alopecia
- Infection risk
- Cardiotoxicity
Key clinical trials
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:
- PAx5/PCMx5 CI brief — competitive landscape report
- PAx5/PCMx5 updates RSS · CI watch RSS
- SWOG Cancer Research Network portfolio CI
Frequently asked questions about PAx5/PCMx5
What is PAx5/PCMx5?
How does PAx5/PCMx5 work?
What is PAx5/PCMx5 used for?
Who makes PAx5/PCMx5?
Is PAx5/PCMx5 also known as anything else?
What drug class is PAx5/PCMx5 in?
What development phase is PAx5/PCMx5 in?
What are the side effects of PAx5/PCMx5?
Related
- Drug class: All Multi-agent chemotherapy regimen drugs
- Manufacturer: SWOG Cancer Research Network — full pipeline
- Therapeutic area: All drugs in Oncology
- Indication: Drugs for Hematologic malignancies (specific indication dependent on SWOG trial protocol)
- Also known as: Lansoprazole: Prevacid
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing