Integrating Science, Care, and Innovation for Better Health  |  312-225-3916  |  keog@kclgmedical.com
GCP Certified MHRA Compliant NHS Partner ClinicalTrials.gov Registered

For Clinicians & Healthcare Professionals

Whether you want to refer a patient, join as an investigator site, access evidence briefings, or explore a research partnership — this page is your starting point.

Refer a Patient to Our Trials

If you have a patient who may be eligible for one of our active studies, here is how to refer quickly and what to include.

KCLG-HAEM-01 · Currently Recruiting

Statin + Ibrutinib in Relapsed/Refractory CLL/SLL

Consider referring if your patient: has R/R CLL or SLL, is on or eligible for ibrutinib, is treated at an NHS haematology centre, has no contraindication to statin therapy, and has adequate performance status (ECOG 0–2).

● Recruiting Phase II · Haematology
KCLG-GEN-02 · Currently Recruiting

Biomarker-Guided Precision Oncology Platform Trial

Consider referring if your patient: has a solid tumour with ≥1 prior line of therapy, has adequate tumour tissue for molecular profiling, has ECOG PS 0–2, and is treated at or can be referred to a participating site.

● Recruiting Phase II · Precision Oncology

How to Refer

  • 1
    Send a brief clinical summary Email research@kclgmedical.com with the patient's diagnosis, current treatment, line of therapy, performance status, and the trial you are enquiring about. A one-paragraph summary is sufficient at this stage.
  • 2
    We assess eligibility and respond within 1 working day Our research team will review the summary against the protocol eligibility criteria and come back to you with a clear yes/possible/no — and next steps if eligible.
  • 3
    Patient information and consent If eligible, we will send you a participant information sheet and consent form to share with your patient. We can also speak directly with the patient if they prefer.
  • 4
    Screening and enrolment Screening visits are arranged at a convenient participating site. We keep you informed throughout and provide you with regular updates on your patient's trial status (with their consent).
Email research@kclgmedical.com Call 312-225-3916

Join as an Investigator Site

We work with NHS Trusts and academic centres as participating sites for our trials, offering full site management support so you can focus on clinical care and research delivery.

What We Provide

Full Site Management Support

  • Ethics and MHRA regulatory submission support
  • R&D office liaison and NHS approval navigation
  • Site initiation visits and investigator training (GCP-compliant)
  • Remote and on-site monitoring
  • Electronic data capture system access and training
  • Investigator brochures, protocol summaries, and patient materials

What We Ask

Site Requirements

  • Named Principal Investigator with relevant clinical expertise
  • Dedicated research nurse or Clinical Research Coordinator (CRC)
  • R&D department willing to review and grant NHS Trust approval
  • Sufficient patient population to meet site recruitment targets
  • Commitment to data quality and protocol adherence

Evidence Briefings & Resources

We translate our research findings — and the broader oncology evidence base — into clear, clinician-focused briefings designed for busy clinical practice.

Monthly Briefing

KCLEAGENICS Monthly Clinical Intelligence Briefing

A curated monthly digest of trial updates, methodology commentary, and practice-relevant evidence reviews — written for NHS consultants, registrars, and specialist nurses.

Evidence Reviews

Oncology Evidence Reviews

Structured summaries of landmark trials and meta-analyses relevant to our research areas — haematological malignancies, precision oncology, immunotherapy, and cancer risk.

Trial Updates

Progress Reports from Active Trials

Regular updates on recruitment progress, interim safety data, and protocol amendments for all KCLEAGENICS MEDICAL active studies — shared with referring clinicians and site investigators.

How We Work With Clinicians

🔬

Co-Investigator

Join our trial as a named co-investigator — contributing to protocol development, patient recruitment at your site, and, where appropriate, co-authorship of publications.

Discuss co-investigator arrangements →

🏥

Referring Clinician

Refer eligible patients to our studies without taking on trial management responsibilities. We handle all research administration and keep you informed of your patient's progress.

How to refer →

🎓

Academic Collaboration

If you hold research funding or are developing a grant application, we can provide the regulatory, operational, and statistical infrastructure to turn your proposal into a running trial.

Academic enquiries →

Ready to Collaborate?

Contact our research team — we will respond within 1 working day.

Email research@kclgmedical.com Call 312-225-3916