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Our models / Outpatient CAR-T
Current Health for CAR-T pairs hands-free toxicity detection with 24/7 support from nurses drawn from ED and ICU, who assess, coordinate, treat, and escalate per your protocol. Academic cancer centers and community practices use it to send nearly every patient home, or to nearby lodging, safely, without adding overnight staff.
90%
of CAR-T patients made eligible for outpatient care (Sarah Cannon)
80%+
of patient issues resolved without escalating to your team
1,500+
advanced therapy episodes
60
peer-reviewed papers and abstracts
Hands-free for patients
Built for the highest-risk weeks after infusion. Patients wear the devices and rest, with nothing to log or remember. Signals stream to our platform day and night, alarms go straight to our nurses, and each day brings a short nurse-led ICE assessment and a few symptom questions on the tablet.
Worn on the upper arm. Passively tracks heart rate, respiratory rate, SpO₂, skin temperature, and activity.
Passive temperature monitoring, so a fever trend shows hours before a spot check would.
Cellular connectivity so no home Wi-Fi is needed. Video calls, symptom check-ins, and virtual ICE assessments run on the tablet, in 50+ languages.
Blood pressure readings to catch hypotension, which moves CRS to Grade 2 or higher.
Delivering bispecifics? See Current Health for Bispecifics →
Our experience
Our outpatient CAR-T model runs in academic medical centers, health systems, and community practices today.
1,500+
advanced therapy episodes
20,000+
advanced therapy patient monitoring days
7
approved CAR-T products supported
Defining the model
Together, we have developed, tested, and published the model for outpatient CAR-T. Our research supports a risk-adapted approach that aims to detect adverse events early, concentrate monitoring when risk is highest, and keep older and frail patients engaged.
We power the largest multisite outpatient CAR-T program, one consistent model across academic, health system, and community sites of different sizes and geographies, extended across five products.
In our study with Sarah Cannon of 209 outpatient CAR-T patients, 98% of CRS and 96% of ICANS began within 15 days of infusion, so programs can focus monitoring where risk is highest.
Continuous multi-parameter signals feed patented CRS detection, and a purpose-built virtual ICANS workflow catches neurotoxicity between visits.
We support CAR-T trials and real-world studies of outpatient administration, generating safety evidence that informs outpatient protocols, site-of-care decisions, and label expansion studies.
24/7 Clinical Coordination Center
We pair every patient with our Clinical Coordination Center. Our nurses, drawn from ED and ICU, are licensed in all 50 states, work with live translation, and present as your program, resolving 80% or more of patient issues without escalating to your team.
01
Temperature, heart rate, respiratory rate, and SpO₂ reach our platform around the clock, with no patient input.
02
Rules agreed with your team look for sustained trends and combined signs, so a single noisy reading doesn't trigger a call.
03
Our nurse reviews the alarm and calls the patient and caregiver. Nurses also round proactively each evening, not only when an alarm fires.
04
Where your standing orders allow, our nurses start treatment at home, such as antipyretics or Grade 1 CRS care, and follow up the next morning, with no overnight call to your team.
05
Anything outside your orders goes to your on-call clinician or to a direct admission at your hospital or partner hospital, with the receiving team called ahead.
2 min
to reach a patient or caregiver about an alarm
80%+
of patient issues resolved by our nurses without site escalation
Sarah Cannon
55%
of clinical alerts occur in the 8 overnight hours
Sarah Cannon
Patients and caregivers
BEFORE INFUSION
The kit arrives ready to use. A nurse calls to welcome the patient, walk through setup, capture baseline vitals, and teach caregivers what to watch for and when to call.
DAY AND NIGHT
Monitoring is passive, so caregivers don't stay up taking readings or checking vital signs. A nurse checks in each evening, and caregivers can call us any time they notice confusion, trouble finding words, or anything else that worries them.
ON SCHEDULE
At the intervals your protocol sets, a nurse runs a short ICE assessment by video, and the patient answers a few symptom questions on the tablet.
IF SOMETHING CHANGES
Within minutes, following the care team's plan. If the patient needs to be seen, we coordinate the visit and call ahead so the receiving team is expecting them.
ANY TIME
Patients and caregivers can reach a nurse with any question.
“Thank you for the support given by the whole team during this period of recovery after the CAR-T cell transplant. God bless you!”
CAR-T patient
HCA Healthcare (translated from Spanish)
After-hours care, by protocol
At Atrium Health Levine Cancer Institute, patients receiving cilta-cel were monitored with Current Health. Under the institution's after-hours protocol, patients with Grade 1 CRS and no ICANS were treated at home or in local lodging after a nurse assessment, with a nurse call-back at about an hour and a clinic visit the next morning. Patients with Grade 2 or higher CRS, or any ICANS, went to the ED.
48%
(10 of 21) had CRS managed after hours with no overnight hospital admission
0
median inpatient days (mean 0.9 per patient)
Your care team
Outpatient CAR-T shouldn't mean more pages for your physicians or a new overnight staffing model. Our model fits around the way your program already works.
We onboard, educate, and set up every patient. EHR enrollment is available but not required.
Thresholds, escalation criteria, and standing orders are set with your physician and nursing leads before go-live. Your physicians decide on treatment and site of care, and our nurses act only under orders you approve.
Our nurses handle routine alarms and patient calls, overnight included, so your clinicians hear only about verified events.
Every call and escalation is documented, with notes written back to your chart once you integrate. Program dashboards track toxicity, escalations, admissions, and patient experience by site and therapy.
Launch support included. We handle protocols, workflows, training, and go-live with your team. Programs already delivering CAR-T are typically live 4–6 weeks from kickoff. You can start at one site, then add sites on the same protocols. Building a new program? Site enablement supports you from the business case through FACT accreditation preparation and manufacturer site qualification, with about six months to first patient.
85%
of patient issues managed without provider escalation at UCSF Health
“They're always watching our patients. So we know when we can't be there, Current Health can.”
Tricia Estacio, RN
Director of Nursing, Parnassus Infusion & Apheresis, UCSF Health
For pharma and biotech
The same passive monitoring model that runs commercial outpatient programs supports CAR-T trials, from early phase through label expansion. Sponsors have brought us into more than 15 clinical trials for advanced therapies, Phase I to IV, including a multi-country Phase II multiple myeloma CAR-T study of up to 225 participants across 40 sites. Monitoring is adapted to each asset with the safety oversight your protocol requires, and smaller sites can take part without building their own overnight coverage.
Duration and intensity set to when the asset's toxicities are expected to appear, including later-onset neurotoxicity.
Device configuration, alarm thresholds, and ePRO instruments matched to the asset's safety profile and protocol endpoints.
Every trial site follows one pre-agreed escalation protocol. Each alarm, contact, and escalation is timestamped and shared with the investigator for adverse event reporting.
Timestamped data with 21 CFR Part 11 audit trails delivered to the EDC you already use. Data quality is watched for every participant, gaps are flagged in real time, and unresolved gaps are followed up by our Clinical Coordination Center.
Access expansion and patient support programs bring the same model to sites that choose to offer your therapy, with consented, deidentified data on hospitalization and bed days.
Any-grade CRS was 83% outpatient vs. 85% inpatient (P = .89) in 143 CD19 CAR-T patients.
Research highlights
Our clinical research team works with partner sites to define, test, and publish how CAR-T can be delivered safely outside the hospital.
83% vs. 85%
any-grade CRS outpatient vs. inpatient, no significant difference (P = .89)
98% · 96%
of CRS and ICANS events, respectively, occurred within the first 15 days
97 to 100%
30-day survival across four sites
60 peer-reviewed papers and abstracts since 2023.
Explore our clinical researchFAQ
Who decides which patients go outpatient?
Your team sets eligibility. We don't gate referrals.
Do patients or caregivers have to take readings?
No. Monitoring is passive. The wearable and temperature patch track vital signs continuously.
Who responds overnight?
Our nurses, drawn from ED and ICU, respond 24/7 and escalate to your on-call clinician per your protocol.
Do we need an EHR integration?
No. It's available if you want it.
We'll walk through our outpatient CAR-T model, your protocols, and what it takes to launch.