ClinicalTrials.gg
RecruitingNCT07679412Updated Jul 1, 2026

Evaluation of Safety and Efficacy of Autologous LB-DTK-CMV in Patients With Antiviral-Resistant and Refractory Cytomegalovirus Retinitis.

An interventional study of LB-DTK-CMV in CMV Retinitis, sponsored by LucasBio. Recruiting at 1 site in South Korea. Open to participants aged 19 Years and older. Per ClinicalTrials.gov, last updated 2026-07-01.

Sponsored by LucasBio · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started Apr 2026; still recruiting 6 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
5
Allocation
Not applicable
Ages
19 Years and older
Sex
All
01

Study summary

The goal of this exploratory clinical study is to evaluate the safety and efficacy of Cytomegalovirus-Specific T cells (LB-DTK-CMV) to treat patients diagnosed with antiviral-resistant and refractory cytomegalovirus retinitis. The main questions it aims to answer are:

  • What adverse events occur after the infusion of LB-DTK-CMV?
  • What is the duration of efficacy following treatment?
  • Is there a clinically significant reduction in CMV viral load in plasma and aqueous humor after the infusion?
  • Is there a clinically significant improvement in clinical symptoms after the infusion?

Participants will:

  • Receive two infusions of LB-DTK-CMV at 2x10\^7cells/m\^2 at two-week intervals beginning at the baseline visit (Cycle 1).
  • Take a three-week resting period following completion of Cycle 1.
  • Receive two infusions of LB-DTK-CMV at 2x10\^7cells/m\^2 at two-week intervals beginning three weeks after the last dose of Cycle 1 (Cycle 2).
02

Conditions studied

  • CMV Retinitis

Keywords

  • CMV
  • Retinitis
  • Virus-specific T cells
  • Antiviral-resistant CMV
  • Refractory CMV
  • Hematopoietic Stem Cell Transplantation
  • Solid Organ Transplantation
  • Hematologic malignancy
  • Autoimmune Disease
  • Immunosuppressants
  • Immunosuppressive drugs
03

In context

Cytomegalovirus Retinitis

64 studies on the registry are indexed under Cytomegalovirus Retinitis; 2 are open to participants now.

This study's planned enrollment of 5 is below the median of 106 across 38 interventional studies indexed under Cytomegalovirus Retinitis.

Browse Cytomegalovirus Retinitis studies →

Lead sponsor

LucasBio is the lead sponsor of 7 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
19 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Patients aged 19 years or older who have been diagnosed with CMV retinitis and have undergone hematopoietic stem cell transplantation or solid organ transplantation for the treatment of hematologic , or have received high-dose therapy for the treatment of diseases, and who meet at least one of the following criteria:

    • Patients with persistent or progressive CMV retinitis despite systemic antiviral therapy or intravitreal antiviral treatment.
    • Patients who have showed persistent CMV viremia despite systemic antiviral therapy or developed new CMV retinitis.
    • Patients with CMV UL54 or UL97 mutations associated with antiviral resistance.
    • Patients with adverse effects or toxicities limiting the administration of more than one systemic antiviral drug.
  2. Patients who are pregnant and able to reduce their dosage to 0.5mg/kg/day of Prednisolone (or an equivalent dose) or less.
  3. For women of , those who tested negative on a pregnancy test (blood test) performed on the screening visit.
  4. Individuals who have voluntarily decided to participate in this clinical study and have provided written consent to comply with the restrictions.
  5. Individuals deemed suitable as study subjects through screening tests (vital signs, physical examination, medical and surgical history, , laboratory tests, etc).

Exclusion criteria

Exclusion Criteria:

  1. Individuals who have received treatment with ATG (Antithymocyte Globulin), Campath (Alemtuzumab), or other T-cell monoclonal antibodies within 28 days prior to the first dose.
  2. Individuals who meet any of the following criteria at the time of screening:

    • Uncontrolled hypertension

      • Systolic BP ≥ 160 mmHg or diastolic BP ≥ 100 mmHg despite taking antihypertensive medication.
    • Uncontrolled severe diabetes: Severe diabetes is defined as follows:

      • Severe hyperglycemia with ≥ 10.0%
      • Individuals who have been hospitalized for diabetic ketoacidosis within the past 12 weeks.
      • Individuals who have received emergency treatment or been hospitalized within the past 12 weeks for severe hypoglycemia (glucose \<54 mg/dL) accompanied by seizures and loss of consciousness.
    • Other viral infections

      • Virus (HBV), Virus (HCV)
      • However, patients who are tested negative for HBsAg and positive for Anti-HBcAb are not subject to this exclusion criterion.
    • Tuberculosis
    • Syphilis
    • Moderate or severe liver damage

      • (AST) or Alanin aminotransferase (ALT) > 5 times the (ULN)
    • Chronic kidney disease

      • \< 30mL/min/1.73m\^2
    • Other uncontrolled infections. However, the following cases are considered controlled infections and do not meet the exclusion criteria:

      • Bacterial infection: Patients must be undergoing definitive antibiotic treatment for the infection and must have shown no signs of progression of the infection for 72 hours prior to enrollment in this clinical study.
      • Fungal infection: Patients must be receiving systemic antifungal therapy and must have shown no signs of infection progression for 1 week prior to enrollment in this clinical study.
  3. Patients who have received donor lymphocyte infusion (DLI) within 28 days prior to the scheduled first dose.
  4. Patients with active malignant tumor or uncontrolled recurrence.
  5. Patients with uncontrolled ophthalmic diseases other than CMV retinitis.
  6. Female subjects who are pregnant, breastfeeding, of , or not using appropriate methods.
  7. Patients with a of less than 24 hours at the time of the screening visit.
  8. Patients who have received an product from another clinical study within 24 weeks prior to administration of the investigational product in this study.
  9. Patients deemed ineligible for participation in this clinical study by the investigator.
Terms in these criteria, in plain language(15)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

Autoimmune disease

A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.

Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

Childbearing potential

Able to become pregnant: from the first period until menopause, unless permanently unable to through surgery (removal of the womb, or of both ovaries or both fallopian tubes).

Criteria for people of childbearing potential usually ask for a negative pregnancy test and for contraception during the study and for a time after it.

ECG (electrocardiogram)

A recording of the heart’s electrical activity, taken with stickers on the chest, arms and legs. It takes a few minutes and does not hurt.

HbA1c

A blood test of average blood sugar over the past two to three months, given as a percentage or in mmol/mol. 6.5% (48 mmol/mol) or more is the usual threshold for diabetes, normally confirmed by a second test.

Hepatitis B tests

Hepatitis B is a virus that infects the liver. These are separate tests: HBsAg positive usually means a current infection (a recent vaccination can briefly cause it too); total anti-HBc (HBcAb) positive means an infection now or in the past; HBV DNA measures how much virus is in the blood.

Some studies accept a past infection if HBV DNA is undetectable, sometimes with antiviral medicine during the study. Check what this study allows.

Hepatitis C tests

Hepatitis C is a virus that infects the liver. An HCV antibody test can stay positive after an infection has cleared (and is occasionally positive without one); an HCV RNA test shows whether the virus is there now.

After treatment, hepatitis C counts as cured when HCV RNA is still undetectable 12 weeks or more after the treatment ended. Studies often accept people cured this way.

ALT and AST (liver enzymes)

Two enzymes measured in a routine blood test of the liver. Higher levels can mean the liver is under strain or damaged. SGPT and SGOT are older names for ALT and AST.

Criteria usually give a limit as a multiple of the upper limit of normal (ULN), often higher when cancer has spread to the liver.

ULN (upper limit of normal)

The top of the normal range for a blood test, as set by the laboratory that runs it. Each lab prints its own range next to your result.

“≤ 2.5 × ULN” means the result can be up to two and a half times that top value.

GFR and eGFR (kidney filtering)

GFR (glomerular filtration rate) is how much blood the kidneys filter each minute. It is usually estimated from a blood test — eGFR, by formulas such as CKD-EPI or MDRD — and some studies ask for it to be measured directly instead. Usually given in mL/min/1.73 m².

Check the method, the units and the minimum the study states. A value of 90 or above is in the normal-or-high range, but kidney damage can show in other tests too.

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

Life expectancy

The study doctor’s estimate of how long someone is likely to live. Criteria use it so that people can stay in the study long enough for it to answer its question.

Investigational drug or device

A drug or device being studied in a clinical trial.

It may be new, or already approved and being studied for another use, dose or form. Criteria often leave out people who took part in another study of one within a recent period, commonly 30 days or five half-lives.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
5 participants (estimated)

Study arms

  • Experimental
    Experimental Group (All)

    Biological: LB-DTK-CMV

Interventions

  • BiologicalLB-DTK-CMV

    LB-DTK-CMV is a CMV-specific T cell therapy product derived from a patient (autologous) and is stored frozen in a colorless, transparent freeze-dried vial until thawed into liquid before administration.

06

What researchers measure

Primary outcomes

  1. Viral Load

    CMV viral load testing is performed using plasma and aqueous humor samples. Viral load is measured at the screening visit and weekly for the first 4 weeks after the first dose in Cycle 1 through the resting period, followed by two measurements at 2-week intervals, then once every 4 weeks, and subsequently once every 12 weeks.

    Time frame: From screening through 24 weeks after treatment initiation

  2. Clinical Symptom Assessment

    Clinical symptom assessments include visual acuity test, fundus examination, and optical coherence tomography. However, optical coherence tomography only applies to patients diagnosed with CMV retinitis involving the central retina. Fluorescein angiography (FAG) may also be performed on Visit 1 and 11 if considered necessary by the investigator.

    Time frame: From the screening through 24 weeks after treatment initiation.

  3. Immunogenicity Testing

    Immunogenicity testing using IFN-γ ELISpot assay is performed to quantify CMV-specific T cells and evaluate the persistence and reconstitution of the immune response.

    Time frame: From the screening through 24 weeks after treatment initiation.

  4. Adverse Events

    The investigator must confirm the occurrence of adverse events through medical examinations during regular visits throughout the clinical study period. Adverse events shall be assessed at each visit starting from the administration of the investigational drug at the baseline visit (Visit 3).

    Time frame: From the baseline visit throughout 24 weeks after treatment initiation.

07

Study locations

1 of 1 sites recruiting
  • The Catholic University of Korea Seoul St.Mary's Hospital
    Seoul, 06591, South Korea
    Recruiting
    • Young Hoon Park, MD-PhD · Principal investigator
08

References and documents

Publications

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Individual participant data

Plan to share: Undecided

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Apr 2026 (actual). Primary completion is estimated for Aug 2027, 15 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Jun 25, 2026
First posted
Jul 1, 2026
StartActual
Apr 27, 2026
Primary completionEst.
Aug 14, 2027
CompletionEst.
Aug 14, 2027
Last update
Jul 1, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jul 1, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07679412
Lead sponsor
LucasBio
Responsible party
YoungHoon Park (Professor of Ophthalmology, The Catholic University of Korea) — Principal investigator
First posted
Jul 1, 2026
Start date
Apr 27, 2026
Primary completion
Aug 14, 2027 (estimated)
Completion
Aug 14, 2027 (estimated)
Last update
Jul 1, 2026

Study contacts

Nayoun Kim, Ph.D.
Contact
nkim@lucasbio.com
+82 1040222340
Young Hoon Park, MD-PhD
principal investigator · Department of Ophthalmology, The Catholic University of Korea Seoul St.Mary's Hospital

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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