Healthcare Professionals Report an Adverse Event Contact Global (EN)
Home / Patients & Clinicians

Patients & clinicians

Baxtra does not yet market any medicine. What we can offer today is clear information about our trials, our cleared device, and how to reach a human being here.

None of Baxtra's medicines are approved or available by prescription. BX-101, BX-204, BX-308 and BX-412 are investigational and can currently only be accessed through a clinical trial or, in limited circumstances, expanded access. Nothing on this site is medical advice.

Considering a trial

What our studies involve, who they are for, and how to check whether you are eligible.

Find a study

Understanding your condition

Plain-language background on the four diseases we work on, written with clinicians.

Therapeutic areas

Caregivers

Practical guidance for family members supporting someone taking part in research, including travel and time commitment.

Ask us a question

Patient support

We have no marketed medicine, so we have no co-pay program — but taking part in research should never leave a participant out of pocket. For every Baxtra-sponsored study we cover:

  • All study medicine, devices and study-related procedures, at no cost
  • Travel, parking and, where visits require it, overnight accommodation
  • A stipend for time and inconvenience, set by the ethics committee
  • A dedicated study coordinator you can call directly
  • Continued access after the study for participants who are benefiting

When our first medicine reaches approval, our access and pricing plan will be published before launch rather than after it.

Talk to us

A real person answers these, usually the same day.

Trial questions
trials@baxtra.com · +1 (561) 555-0177

Medical information
medinfo@baxtra.com · +1 (561) 555-0119

Safety reporting
safety@baxtra.com · +1 (561) 555-0142

Report a side effect or device problem

If you are having a medical emergency, call 911 or your local emergency number immediately. This form is not monitored in real time and must not be used for urgent medical help.

You may also report directly to the FDA through MedWatch. Reporting to Baxtra does not replace reporting to the FDA.

For healthcare professionals

Scientific and technical resources intended for licensed clinicians.

Lumavue™ instructions for use

Full labelling, indications, contraindications, warnings and setup guidance for the cleared imaging system.

Device information

Medical information

Submit an unsolicited scientific question about any Baxtra program; answers are evidence-based and referenced.

Ask medical information

Become a study site

We are actively adding sites for our Phase 1 programs and the Lumavue post-market study.

Site enquiries

Surgeon simulation lab

Hands-on sessions with our prototypes at the Palm Beach Gardens facility, open to practising surgeons.

Request a session

Investigator-initiated studies

Apply for support for research you design and sponsor.

Submit a concept

Expanded access

Our policy on providing investigational products outside a clinical trial.

Read the policy

Expanded access (compassionate use)

In limited circumstances a physician may request an investigational Baxtra medicine for a patient with a serious or life-threatening condition who cannot enrol in a trial and has no satisfactory alternative. Requests must come from the treating physician.

What we consider

Whether the available data suggests potential benefit outweighs risk for that patient; whether supply exists; and whether providing the product would compromise the trials needed for approval. With only Phase 1 data on most programs, that third question is currently a real constraint and we will say so plainly.

How to request

The treating physician emails expandedaccess@baxtra.com. We acknowledge within two business days and aim to decide within ten.

Cost

Baxtra does not charge for investigational product supplied under expanded access.