Phastar partnered with an emerging biotech to develop an innovative Bayesian Phase I/II oncology design for a first-in-human clinical trial.
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Launching a first-in-human clinical trial is a major milestone, especially with limited patient numbers and complex regulatory requirements. Phastar partnered with an em…
Company
Phastar
Bringing data to life
- Industry
- Biotechnology Research
- Location
- London, GB
- Company size
- 201–500 employees
About Phastar
Phastar is an award-winning specialist biometrics and data science CRO, trusted by pharma, biotech, and medical device companies worldwide. With a global team of data specialists, it brings expertise, precision, and pace to every trial – because behind every data point is a patient waiting for treatment. Phastar doesn’t just deliver high-quality clinical trial data. It partners with clients to turn complexity into clarity. Leveraging technology, AI-enhanced analytics, advanced statistical methods, and deep therapeutic expertise, it accelerates regulatory approvals, ensures compliance with global standards and mitigates risk. Phastar has a proven track record in transforming complex data into clear, actionable intelligence, empowering its partners to accelerate drug development. With scalable, tailored solutions, it expedites trials – bringing life-changing therapies to patients faster.
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Latest activity from Phastar
9 signals
Presence & Recognition
Phastar is attending the ASA Biopharmaceutical Section Regulatory-Industry Statistics Workshop in Rockville, MD, at Booth #13.
Presence & Recognition
Phastar's Principal Data Scientist Evgeny Galimov will be presenting at CLAIR 2026 on how AI and self-service approaches can help bridge the gap between research questions and actionable evidence in clinical research.
Research & Knowledge
Phastar published a case study detailing how the company designed a Bayesian Phase I/II trial for an emerging biotech preparing for its first-in-human oncology study to support dose escalation, early efficacy assessment, and regulatory acceptance from both the FDA and EMA.
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