Your specialist somatic genomics and clinical trial navigation partner
We provide your patients with expert-led trial matching, somatic genomic testing, and actionable reports, saving your clinical time while expanding their options. Explore our direct-to-patient services below, or contact us to discuss referring your patients directly to RareCan.
Refer your patients directly
Would you like to refer patients directly to RareCan? Contact us to discuss partnering with RareCan to provide clinical trial and genomics support directly to you.
Partner with RareCanOur clinical trial support services:
Trial Navigation Call
Helping patients understand clinical trials and whether / when they might be an option £50
- 30 minute call with an experienced Trial Navigator
- Review patient's current situation and treatment
- Discuss whether / when trials might be a option
- Explanation of UK cancer trials and how they work
- £50 credit towards Personalised Report or InsightDecode
InsightDecode
Advanced trial matching based on existing genetic test results, plus UK-actionalble treatment options £250
- Everything in the Personalised Report
- Bespoke trial matching based on known genetic alterations
- Translation of existing genetics report into plain English summary
- Expert review of treatment and trial options
Our Insight genomic tests:
Insight TSB
Targeted genomic profiling of solid tumours from blood £2,200
- SNVs & InDels across 118 genes
- Fusions in 15 genes
- Tumour fraction estimate (TFx)
- Sequencing depth >20,000x
- UK-actionable treatment and trial options
Insight PCB
Precision genomic profiling of colorectal cancers from blood £2,500
- SNVs & InDels across 31 genes
- CNVs across 12 genes
- Fusions in 9 genes
- MSI, TMB
- Tumour fraction estimate (TFx)
- Sequencing depth >20,000x
- UK-actionable treatment and trial options
Supported by
Our Partners
Regulatory Compliance
