A Dose-Escalation Study Evaluating Safety and Tolerability of Viral-Specific T Cells Against CMV in Adult Solid Organ Transplant Recipients

Cytomegalovirus Infections Clinical Trial

Official title:

A Phase I Dose-Escalation Study Evaluating Safety and Tolerability of Viral-Specific T Cells Against CMV in Adult Solid Organ Transplant Recipients

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT03950414
• Other study ID #: 2019-0060
• Secondary ID: PACT VST-C-002Pr
• Status: Terminated
• Phase: Phase 1
• Start date: September 27, 2019
• Est. completion date: July 11, 2022

Study information

• Verified date: February 2024
• Source: University of Wisconsin, Madison
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study measures the tolerability of viral-specific T cells against Cytomegalovirus (CMV) in adult solid organ transplant (SOT) recipients. Participants are expected to be on study for 52 +/- 3 weeks.

Description:

Viral infections, or their reactivation in the immunocompromised host, remain serious complications that adversely affect outcomes of transplantation. These infections may be refractory to pharmacologic treatment and result in increased morbidity and mortality after transplantation. Furthermore, the available pharmacologic therapies can result in severe toxicities.

Once an infection occurs, adequate immune reconstitution is decisive for recovery from viral disease after solid organ transplantation. The present trial will consist of the treatment of solid organ transplant recipients diagnosed with severe CMV infection when standard antiviral therapy is ineffective (disease progression on therapy, decline in viral load less than 10-fold in 2 weeks, known drug resistance), or toxic (end-organ damage), with virus-specific T cells using the CliniMACS® Prodigy System. These are the patients with the greatest unmet need and greatest risk or morbidity and allograft loss due to CMV infection. CMV-specific T cells will be isolated from donor leukapheresis products using the CliniMACS® Prodigy. Prior studies on transfer of CMV-specific T cells have been shown to be safe and efficacious in the treatment of CMV infections.

The primary objective of this Phase I trial is to evaluate the safety and tolerability of CMV-specific T-cell transfer in adult patients suffering from CMV infections following solid organ transplantation using a dose escalation design. The incubation with viral antigens (MACS GMP PepTivator) allows the enrichment of CMV-specific CD4+(Cluster of Differentiation 4) and CD8+(Cluster of Differentiation 8) T cells. Increasing evidence of the safety and efficacy of CMV-specific T-cell is available. Furthermore, the safety and efficacy of the specific manufacturing approach using the fully automated protocol of the ClinMACS® Prodigy for the isolation of CMV-specific T cells against CMV has been described and demonstrated that these cells retain their biological properties.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 2
• Est. completion date: July 11, 2022
• Est. primary completion date: July 11, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

1. Adult (age = 18 and =75) patients suffering from CMV reactivation/infections following solid organ transplantation (e.g., liver, pancreas, lung, heart, and multi-solid organ)

• CMV reactivation/viremia defined as positive (>250 copies/mL) CMV qPCR(quantitative polymerase chain reaction) AND/OR

• Presence of symptoms secondary to CMV infection or evidence of invasive CMV infection (e.g. pneumonitis, colitis)

AND ONE OF THE FOLLOWING CRITERIA:

• Absence of an improvement of viral load after = 14 days of standard antiviral therapy with ganciclovir, valganciclovir or foscarnet (decrease by at least 1 log, i.e. 10-fold), or

• New, persistent and/or worsening CMV-related symptoms, signs and/or markers of end organ compromise while on anti-viral therapy with medications such as ganciclovir, acyclovir, valganciclovir, foscarnet, cidofovir, IVIG(Intravenous immunoglobulin), and/or letermovir, or

• Have contraindications or experience adverse effects of anti-viral therapy with medications such as ganciclovir, acyclovir, valganciclovir, foscarnet, cidofovir, IVIG, and/or letermovir, or

• Known resistance to the anti-viral medications ganciclovir, foscarnet and/or cidofovir based on molecular testing

2. Availability of eligible donor

3. Written informed consent given by patient

Exclusion Criteria:

1. Patient with acute rejection of allograft at time of T-cell transfer

2. Patient receiving steroids (>0.5 mg/kg body weight (BW) prednisone equivalent) at the time of T-cell transfer

3. Patient treated with Thymoglobulin (ATG), Alemtuzumab or T-cell immunosuppressive monoclonal antibodies within 28 days

4. Patients with CMV retinitis

5. Concomitant enrollment in another clinical trial interfering with endpoints of this study

6. Any medical condition which could compromise participation in the study according to the investigator's assessment

7. Known HIV infection

8. Female patient who is pregnant or breast-feeding, or adult of reproductive potential not willing to use an effective method of birth control during study treatment Note: Women of childbearing potential must have a negative serum pregnancy test at study entry.

9. Patients unwilling or unable to comply with the protocol or unable to give informed consent

Donor Eligibility

Donor selection priority: The original donor will be the first choice as the source of T cells. If donation from the original organ donor is not possible (e.g., donor is unavailable or ineligible), then an alternative related donor will be selected, with preference for those who have full HLA matching in 6/6 loci over those with partial HLA matching (= 2/6 HLA loci). See Appendix 1 for patient and donor screening procedures.

1. = 18 years old

2. Available and capable of undergoing a single standard 2 blood volume leukapheresis or donation of one unit of whole blood.

3. If the original transplant donor is not eligible, then an eligible fully matched or eligible partially matched family member will be used as the donor.

4. Related donors must be at least partially HLA compatible, matching with recipient in at least 2/6 HLA loci (HLA-A, HLA-B and HLA-DRB1 will be considered for this).

5. Donors must be CMV IgG seropositive.

6. Donors must show CMV T-cell activation after incubation with MACS GMP PepTivator Peptide Pools of CMV pp65 before undergoing leukapheresis.

7. Donor must meet the criteria for donor selection defined in the UWHC Hematopoietic Stem Cell Transplant Program SOP and FACT standards, which comply with 21 CFR 1271, subpart C.

8. Donor must provide written informed consent.

Related Conditions & MeSH terms

• Cytomegalovirus Infections
• Solid Organ Transplant

Intervention

Biological:
• CMV specific T-cells
Naturally occurring, allogeneic donor lymphocytes derived from a leukapheresis or a whole blood product, enriched for CMV-specific CD4+ and CD8+ T cells Suspension of CMV-specific T cells in 10 mL of 0.9% NaCl with 2% Human Serum Albumin(HSA) via IV bolus injection Low Dose Tier - Viral-Specific T cell infusion 5 x10^3 cells/kg body weight(BW) Mid Dose Tier - Viral-Specific T cell infusion 1.25 x10^4 cells/kg BW High Dose Tier - Viral-Specific T cell infusion 2.5 x10^4 cells/kg BW Product will be administered fresh intravenously to recipient within four hours of collection.

Locations

Country	Name	City	State
United States	University of Wisconsin School of Medicine and Public Health	Madison	Wisconsin

Sponsors (1)

Lead Sponsor	Collaborator
University of Wisconsin, Madison

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Safety and Tolerability:Time of Occurence of Acute GVHD	Time to occurrence of acute GVHD of any grade will be evaluated using the Kaplan-Meier method to assess incidence and severity of acute GVHD from day of T-cell transfer. The first day of GVHD onset at a certain grade will be used to calculate a cumulative incidence curve for that GVHD grade. Overall, cumulative incidence curves will be computed along with the 95% confidence intervals until Week 12 after T-cell transfer with death considered as a competing risk.	up to 15 weeks
Primary	Safety and Tolerability: Number of infusion-related adverse events	Incidence of grades 3-5 infusion-related adverse events, grades 4-5 non-hematological adverse events within four weeks of the CMV-VST dose that are not due to the pre-existing infection or original malignancy or pre-existing co-morbidities	up to 7 weeks
Primary	Incidence of acute infusion-related toxicity	Incidence of acute infusion-related toxicity as assessed by maximum toxicity on the day of T-cell transfer, evaluated by measuring vital signs prior to and at different times after the T-cell transfer and monitoring of specific adverse events (chills, nausea, vomiting, diarrhea, abdominal pain, allergic reactions, respiratory dysfunction or headache from T-cell transfer to 4 hours post injection)	from T-cell transfer to 4 hours post injection, upto 3 weeks
Primary	Severity of acute infusion-related toxicity as measured by Cytokine release syndrome (CRS) Grading criteria	Severity of acute infusion-related toxicity will be assessed by CRS grading criteria.; Grade 1 Symptoms are not life threatening and require symptomatic treatment only, (e.g., fever, nausea, fatigue, headache, myalgias, malaise) Grade 2 Symptoms require and respond to moderate intervention Grade 3 Symptoms require and respond to aggressive intervention Grade 4 Life-threatening symptoms Grade 5 Death; Any grade 3 or greater occurrence of CRS will be considered a serious adverse event for this study.	from T-cell transfer to 4 hours post injection, upto 3 weeks
Primary	Number of Participants of Newly Occurring Acute Rejection after T-cell Transfer	Incidence and severity of acute rejection of the organ allograft will in part be measured by number of participants of newly occurring acute rejection after T-cell transfer	up to 15 weeks
Primary	Incidence of de novo Antibodies against Organ Allograft Donor (dnDSA) after T-cell Transfer	Incidence and severity of acute rejection of the organ allograft will in part be measured by presence of de novo antibodies against organ allograft donor (dnDSA) after T-cell transfer	up to 55 weeks
Primary	Incidence of GVHD Grade =1	Incidence and severity of Graft-versus-host disease (GVHD) will be measured by occurrence of acute GVHD grade =1 or aggravation of pre-existing acute GVHD after T-cell transfer	up to 15 weeks
Secondary	Feasibility: Was production of CMV Virus specific T lymphocyte (VST) from donors accomplished?	There is no minimum cell count required for the study as it can vary. Successful production of CMV Virus specific T lymphocyte (VST) from donors will be tracked by a Yes/No question.; Production of cell accomplished: yes/no	up to 3 weeks
Secondary	Feasibility: Participant Drop-out rate	Evaluation of feasibility of CMV specific T cell transfer in adult patients suffering from severe CMV infection following solid organ transplantation in part will be measured by participant drop out rate	up to 3 weeks
Secondary	Feasibility: Time from patient inclusion to administration of CMV-VST	Evaluation of feasibility of CMV specific T cell transfer in adult patients suffering from severe CMV infection following solid organ transplantation in part will be measured by the amount of time from patient inclusion to administration of CMV-VST	up to 21 days
Secondary	Efficacy: Percentage of patients with =1 log decrease in CMV viral load	Evaluation of efficacy of CMV-specific T-cell transfer in adult patients suffering from severe CMV infection following solid organ transplantation in part will be measured in terms of percentage of patients with =1 log decrease in CMV viral load at Week 12	up to 15 weeks
Secondary	Efficacy:Time to 1 log change in CMV viral load	Evaluation of efficacy of CMV-specific T-cell transfer in adult patients suffering from severe CMV infection following solid organ transplantation in part will be measured in terms of time to 1 log change in CMV viral load	up to 15 weeks
Secondary	Efficacy:Number of Participants with CMV clearance	Efficacy evaluation in part will be measured by number of participants with CMV clearance. Either negative polymerase chain reaction (PCR) or <250 copies/mL will be considered as CMV clearance.	up to 15 weeks
Secondary	Efficacy: Time of clearance of CMV	Efficacy evaluation in part will be measured by number of days to achieve CMV clearance. Either negative polymerase chain reaction [PCR] or <250 copies/mL)will be considered as CMV clearance.	up to 55 weeks
Secondary	Efficacy: Number of participants having CMV reactivation	Efficacy in part will be measured by number of participants with CMV reactivations following initial viral clearance	up to 55 weeks
Secondary	Efficacy: Overall Survival of Participant	Overall survival rate of participants will be measured by time from T-cell transfer to death, graft loss, or last follow-up throughout the study	up to 55 weeks
Secondary	Efficacy:Number of Participants with Clinical response/resolution of symptoms of underlying viral infection	Efficacy in part will be measured by number of patients with resolution of clinical symptoms of underlying CMV infection from Day 7 (Week 1) to Week 12 after T-cell transfer as compared to Day 0	up to 15 weeks