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Open single period A140
Open single period A140 is a CD47 inhibitor Small molecule drug developed by Sichuan Kelun-Biotech Biopharmaceutical Co., Ltd.. It is currently in Phase 3 development for Relapsed or refractory acute myeloid leukemia, Relapsed or refractory non-Hodgkin lymphoma. Also known as: KL-140.
A140 is a monoclonal antibody targeting CD47.
A140 is being studied as a potential treatment for metastatic colorectal cancer in a Phase III clinical trial. In this trial, the efficacy and safety of A140, combined with mFOLFOX6, are being compared to Erbitux in patients with Ras wild-type metastatic colorectal cancer.
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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 | Open single period A140 |
|---|---|
| Also known as | KL-140 |
| Sponsor | Sichuan Kelun-Biotech Biopharmaceutical Co., Ltd. |
| Drug class | CD47 inhibitor |
| Target | CD47 |
| Modality | Small molecule |
| Therapeutic area | Oncology |
| Phase | Phase 3 |
Mechanism of action
CD47 is a protein that inhibits phagocytosis, and by blocking it, A140 aims to enhance the immune system's ability to recognize and destroy cancer cells. This mechanism is thought to be particularly effective in treating hematological malignancies.
Approved indications
- Relapsed or refractory acute myeloid leukemia
- Relapsed or refractory non-Hodgkin lymphoma
Common side effects
- Neutropenia
- Thrombocytopenia
- Anemia
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:
- Open single period A140 CI brief — competitive landscape report
- Open single period A140 updates RSS · CI watch RSS
- Sichuan Kelun-Biotech Biopharmaceutical Co., Ltd. portfolio CI
Frequently asked questions about Open single period A140
What is Open single period A140?
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Related
- Drug class: All CD47 inhibitor drugs
- Target: All drugs targeting CD47
- Manufacturer: Sichuan Kelun-Biotech Biopharmaceutical Co., Ltd. — full pipeline
- Therapeutic area: All drugs in Oncology
- Indication: Drugs for Relapsed or refractory acute myeloid leukemia
- Indication: Drugs for Relapsed or refractory non-Hodgkin lymphoma
- Also known as: KL-140
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing