Last reviewed · How we verify
Iptilimumab
Iptilimumab is a Small molecule drug developed by InSightec. It is currently in Phase 3 development.
Iptilimumab is not mentioned in the provided facts. However, based on the information, a 2-sentence factual summary of the study involving pembrolizumab and atezolizumab can be written as follows: Pembrolizumab and atezolizumab are being studied in combination with blood-brain barrier opening using Exablate focused ultrasound for the treatment of non-small cell lung cancer brain metastases. This study, led by InSightec, aims to assess the safety and efficacy of this treatment approach in patients with NSCLC brain mets.
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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).
| 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 | Iptilimumab |
|---|---|
| Sponsor | InSightec |
| Modality | Small molecule |
| Therapeutic area | Other |
| Phase | Phase 3 |
Approved indications
Common side effects
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:
- Iptilimumab CI brief — competitive landscape report
- Iptilimumab updates RSS · CI watch RSS
- InSightec portfolio CI
Frequently asked questions about Iptilimumab
What is Iptilimumab?
Who makes Iptilimumab?
What development phase is Iptilimumab in?
Related
- Manufacturer: InSightec — full pipeline
- Therapeutic area: All drugs in Other
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing