A Study on Cytomegalovirus (CMV) Infection Outcomes Among Solid Organ Transplant (SOT) Participants in Europe and Canada

Cytomegalovirus (CMV) Clinical Trial

Official title:

A Multinational, Non-Interventional, Retrospective Study on CMV Infection Outcomes, Treatment Patterns and Healthcare Utilization Study (OTUS) Among Solid Organ Transplant (SOT) Recipients in Europe and Canada (OTUS SOT Extension in the EUCAN Countries: Austria, Belgium, Canada, Greece, Israel, Italy, Netherlands, Poland and Sweden)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05576805
• Other study ID #: TAK-620-4003
• Status: Completed
• Start date: June 19, 2023
• Est. completion date: March 31, 2024

Study information

• Verified date: April 2024
• Source: Takeda
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The main aim of the study is to assess the clinical outcomes of current CMV management across different regions of the world (Europe [EU] and Canada [CAN]). Data will be collected retrospectively from medical charts.

No study medicines will be provided to participants in this study.

Description:

This study consists of two cohorts: Cohort 1 (resistant, refractory or intolerant to anti-CMV agents) includes participants who had an SOT after January 1, 2016. Cohort 2 (pre-emptive treatment for CMV viremia) includes participants who had an SOT after January 1, 2019. Participants who meet the criteria for both cohorts will be evaluated in each cohort separately (i.e., Cohort 1 and Cohort 2 are not mutually exclusive, and participants will be analyzed in both cohorts using unique index dates with respect to the cohort-specific eligibility criteria). Participant follow-up in the medical record must be available for at least one year from the CMV index date or death, whichever occurs first. The start date of data collection corresponds to the end of participant follow up. For Cohort 1, it is expected that follow-up data will be available for up to 7 years (for those participants with an index date in 2016 and followed through 2022). For Cohort 2, it is expected that follow-up data will be available for up to 4 years (for those participants with an index date in 2019 and followed through 2022).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 159
• Est. completion date: March 31, 2024
• Est. primary completion date: March 31, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

(Cohort 1) Resistant / Refractory or Intolerant:

1. Aged greater than or equal to (>=) 18 years at the time of the SOT.

2. Received an SOT after January 1, 2016.

3. Diagnosed with asymptomatic or symptomatic CMV infection any time after the SOT date.

4. Required >=1 anti-CMV agent to manage CMV infection and were subsequently considered:

1. resistant to currently available anti-CMV agent; OR

2. refractory to currently available anti-CMV agent; OR

3. intolerant to currently available anti-CMV agent.

5. Follow-up information is available for at least 12 months from the index date (that is, date when the participant was first considered resistant, refractory or intolerant to anti-CMV agent) or death, whichever occurs first.

6. Provided written informed consent prior to the initiation of any study procedures (unless waiver was granted by the Institutional Ethical Committee [IEC]).

(Cohort 2) Pre-emptive treatment for CMV viremia:

1. Aged >=18 years at the time of the SOT.

2. Received an SOT after January 1, 2019.

3. Diagnosed with CMV viremia any time after the SOT date and received pre-emptive anti-CMV agent.

4. Follow-up information is available for at least 12 months from the index date (that is, date when the participant was first preemptively treated with an anti-CMV agent) or death, whichever occurs first.

5. Provided written informed consent prior to the initiation of any study procedures (unless waiver was granted by the IEC).

Exclusion Criteria: (Cohorts 1 and 2)

1. Diagnosed as being positive for human immunodeficiency virus before the SOT.

2. Unable to demonstrate a minimum of 12 months of follow-up from the index date (example, incomplete information on dates showing follow-up time).

3. Participation in a clinical trial related to CMV treatment during the study period .

Related Conditions & MeSH terms

• Cytomegalovirus (CMV)
• Cytomegalovirus Infections

Locations

Country	Name	City	State
Austria	MU Graz	Graz
Austria	MU Innsbruck	Innsbruck
Belgium	UZ Leuven	Leuven
Canada	Vancouver GH (VCH)	Vancouver	British Columbia
Greece	Aristotle USM	Thessaloniki
Israel	Rabin Medical Center	Petah Tikva
Italy	U Parma	Parma
Italy	FP Vergata	Roma
Italy	U Insubria	Varese
Netherlands	Erasmus UMC	Rotterdam
Netherlands	UMC Utrech	Utrecht
Poland	UCC Gdansk	Gdansk
Poland	MU Warsaw	Warszawa
Sweden	Karolinska UH	Solna
Sweden	Uppsala UH	Uppsala

Sponsors (1)

Lead Sponsor	Collaborator
Takeda

Countries where clinical trial is conducted

Austria,  Belgium,  Canada,  Greece,  Israel,  Italy,  Netherlands,  Poland,  Sweden, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Time from Solid Organ Transplant (SOT) Until Start Date of the Symptomatic or Asymptomatic Index Episode	Index episode is first CMV episode in which the participant is considered RRI to anti-CMV treatment or had CMV viremia and received pre-emptive treatment, without becoming RRI during that episode. Symptomatic episode is an episode wherein there is "Tissue invasive/end organ disease" or "CMV syndrome" at any time, and asymptomatic when there is no such observation.	From SOT up to start date of the index episode (Up to 7 years 3 months)
Primary	Percentage of Participants who are Asymptomatic and Symptomatic at the Index and Recurrent Episodes	Index episode is first CMV episode in which the participant is considered RRI to anti-CMV treatment or had CMV viremia and received pre-emptive treatment, without becoming RRI during that episode. Recurrent episodes is defined as new CMV infection in a participant with previous evidence of CMV infection. Symptomatic episode is an episode wherein there is "Tissue invasive/end organ disease" or "CMV syndrome" at any time, and asymptomatic when there is no such observation.	Up to 7 years 3 months
Primary	Percentage of Participants With CMV Viremia Clearance as Defined by Site Investigator at the Index Episode and for Recurrent Episodes	Index episode is first CMV episode in which the participant is considered RRI to anti-CMV treatment or had CMV viremia and received pre-emptive treatment, without becoming RRI during that episode. Recurrent episodes is defined as new CMV infection in a participant with previous evidence of CMV infection. CMV viremia clearance is defined as when an active CMV viremia can be considered cleared from the participant, as determined by the site investigator.	Up to 7 years 3 months
Primary	Time From Start of Index Episode to CMV Viremia Clearance as Defined by Site Investigator	Index episode is first CMV episode in which the participant is considered RRI to anti-CMV treatment or had CMV viremia and received pre-emptive treatment, without becoming RRI during that episode. CMV viremia clearance is defined as when an active CMV viremia can be considered cleared from the participant, as determined by the site investigator.	From start of index episode to CMV viremia clearance (Up to 7 years 3 months)
Primary	Percentage of Participants With CMV Viremia Clearance as Defined by Site Investigator at Week 8 After Index Date	Index date is the date when participant was considered resistant, refractory or intolerant to anti-CMV treatment for the first time after transplant (RRI CMV index date) or pre-emptive treatment for the first time after transplant following CMV viremia (CMV preemptive treatment index date). CMV viremia clearance is defined as when an active CMV viremia can be considered cleared from the participant, as determined by the site investigator. The assessment will be based on Kaplan-Meier estimate.	At Week 8 after index date
Primary	Percentage of Participants With CMV Viremia Clearance as Defined by Site Investigator at Week 20 After Index Date	Index date is the date when participant was considered resistant, refractory or intolerant to anti-CMV treatment for the first time after transplant (RRI CMV index date) or pre-emptive treatment for the first time after transplant following CMV viremia (CMV preemptive treatment index date). CMV viremia clearance is defined as when an active CMV viremia can be considered cleared from the participant, as determined by the site investigator. The assessment will be based on Kaplan-Meier estimate.	At Week 20 after index date
Primary	Percentage of Participants With CMV Viremia Clearance as Defined by Site Investigator at 1-year After Index Date	Index date is the date when participant was considered resistant, refractory or intolerant to anti-CMV treatment for the first time after transplant (RRI CMV index date) or pre-emptive treatment for the first time after transplant following CMV viremia (CMV preemptive treatment index date). CMV viremia clearance is defined as when an active CMV viremia can be considered cleared from the participant, as determined by the site investigator. The assessment will be based on Kaplan-Meier estimate. Non-detectable CMV is defined as highest minimum detectable level of CMV assays across all sites.	At 1-year after index date
Primary	Percentage of Participants With Non-detectable CMV During the Index Episode Prior to and After the Index Date	Index episode is first CMV episode in which the participant is considered RRI to anti-CMV treatment or had CMV viremia and received pre-emptive treatment, without becoming RRI during that episode. Index date is the date when participant was considered resistant, refractory or intolerant to anti-CMV treatment for the first time after transplant (RRI CMV index date) OR pre-emptive treatment for the first time after transplant following CMV viremia (CMV preemptive treatment index date). The assessment will be based on Kaplan-Meier estimate.	Up to 7 years 3 months
Primary	Percentage of Participants With Evidence of Non-detectable CMV at Week 8 After Index Date	Index date is the date when participant was considered resistant, refractory or intolerant to anti-CMV treatment for the first time after transplant (RRI CMV index date) or pre-emptive treatment for the first time after transplant following CMV viremia (CMV preemptive treatment index date). Non-detectable CMV is defined as highest minimum detectable level of CMV assays across all transplant sites. The assessment will be based on Kaplan-Meier estimate.	At Week 8 after index date
Primary	Percentage of Participants With Evidence of Non-detectable CMV at Week 20 After Index Date	Index date is the date when participant was considered resistant, refractory or intolerant to anti-CMV treatment for the first time after transplant (RRI CMV index date) or pre-emptive treatment for the first time after transplant following CMV viremia (CMV preemptive treatment index date). Non-detectable CMV is defined as highest minimum detectable level of CMV assays across all transplant sites. The assessment will be based on Kaplan-Meier estimate.	At Week 20 after index date
Primary	Percentage of Participants With Evidence of Non-detectable CMV at 1-year After Index Date	Index date is the date when participant was considered resistant, refractory or intolerant to anti-CMV treatment for the first time after transplant (RRI CMV index date) or pre-emptive treatment for the first time after transplant following CMV viremia (CMV preemptive treatment index date). Non-detectable CMV is defined as highest minimum detectable level of CMV assays across all transplant sites.	At 1-year after index date
Primary	Time From Treatment Initiation to CMV Viremia Clearance as Defined by Site Investigator at the Index Episode	Index episode is first CMV episode in which the participant is considered RRI to anti-CMV treatment or had CMV viremia and received pre-emptive treatment, without becoming RRI during that episode. CMV viremia clearance is defined as when an active CMV viremia can be considered cleared from the participant, as determined by the site investigator.	From Treatment Initiation to CMV Viremia Clearance (Up to 7 years 3 months)
Primary	Time From Treatment Initiation Until Evidence of Non-detectable CMV at the Index Episode	Index episode is first CMV episode in which the participant is considered RRI to anti-CMV treatment or had CMV viremia and received pre-emptive treatment, without becoming RRI during that episode. Non-detectable CMV is defined as highest minimum detectable level of CMV assays across all sites.	Time from treatment initiation until evidence of non-detectable CMV (Up to 7 years 3 months)
Primary	Time from Start of Index Episode to First Symptomatic CMV Diagnosis	Index episode is first CMV episode in which the participant is considered RRI to anti-CMV treatment or had CMV viremia and received pre-emptive treatment, without becoming RRI during that episode. Symptomatic CMV is defined CMV-related tissue invasive disease or CMV syndrome.	From start of index episode to first symptomatic CMV diagnosis (Up to 7 years 3 months)
Primary	Time From Stop Date of the Index Episode to First Recurrent Asymptomatic and Symptomatic CMV Viremia	Index episode is first CMV episode in which the participant is considered RRI to anti-CMV treatment or had CMV viremia and received pre-emptive treatment, without becoming RRI during that episode. Recurrent episodes is defined as new CMV infection in a participant with previous evidence of CMV infection.	From stop date of the index episode to first recurrent asymptomatic and symptomatic CMV viremia (Up to 7 years 3 months)
Primary	Percentage of Participants With Anti-CMV Treatment-related Myelosuppression and Nephrotoxicity	Index episode is first CMV episode in which the participant is considered RRI to anti-CMV treatment or had CMV viremia and received pre-emptive treatment, without becoming RRI during that episode. Percentage of participants with anti-CMV treatment-related myelosuppression each type and nephrotoxicity overall and during the index episode will be reported.	Up to 7 years 3 months
Primary	Percentage of Participants With Organ Rejection From SOT	Organ rejection will include overall and by type (acute, chronic or both for T-cell and anti-body mediated).	Up to 7 years 3 months
Primary	Percentage of Participants With Graft Loss From SOT and the Index Date	Index date is the date when participant was considered resistant, refractory or intolerant to anti-CMV treatment for the first time after transplant (RRI CMV index date) or pre-emptive treatment for the first time after transplant following CMV viremia (CMV preemptive treatment index date. Graft loss is defined as lack of a functioning graft attributable to infection, immunological response in the organ recipient, recurrent disease, or recurrent underlying disease as described in the physician notes.	Up to 7 years 3 months
Primary	Percentage of Participants who Died due to any Cause From SOT and Index Date	Index date is the date when participant was considered resistant, refractory or intolerant to anti-CMV treatment for the first time after transplant (RRI CMV index date) or pre-emptive treatment for the first time after transplant following CMV viremia (CMV preemptive treatment index date, Percentage of participants who died due to any cause from sot and from the index date will be reported.	Up to 7 years 3 months
Primary	Percentage of Participants who Died due to CMV Infection From SOT and Index Date	Index date is the date when participant was considered resistant, refractory or intolerant to anti-CMV treatment for the first time after transplant (RRI CMV index date) or pre-emptive treatment for the first time after transplant following CMV viremia (CMV preemptive treatment index date. Percentage of participants who died due to CMV infection from SOT and the index date will be reported.	Up to 7 years 3 months
Primary	Number of Genetic Mutations Conferring Anti-CMV Resistance From SOT and Index Date	Index date is the date when participant was considered resistant, refractory or intolerant to anti-CMV treatment for the first time after transplant (RRI CMV index date) or pre-emptive treatment for the first time after transplant following CMV viremia (CMV preemptive treatment index date. Genetic mutation includes UL27, UL54, UL56, UL97, other, unknown mutation. Number of genetic mutations conferring anti-CMV resistance from SOT and at index date will be reported.	Up to 7 years 3 months
Primary	Percentage of Participants With a Genetic Mutation Conferring Anti-CMV Resistance From SOT at the Index Date	Index date is the date when participant was considered resistant, refractory or intolerant to anti-CMV treatment for the first time after transplant (RRI CMV index date) or pre-emptive treatment for the first time after transplant following CMV viremia (CMV preemptive treatment index date. Genetic mutation includes UL27, UL54, UL56, UL97, other, unknown mutation. Percentage of participants with genetic mutations conferring anti-CMV resistance from SOT at index date will be reported.	Up to 7 years 3 months
Secondary	Percentage of Participants With Anti-CMV Primary or Secondary Prophylaxis and Preemptive Treatment	Primary Prophylaxis is defined as when the start date of the anti-CMV prophylaxis was prior to start date of first CMV episode. Secondary Prophylaxis is defined as when the start date of the anti-CMV prophylaxis was on/ after the end date of the previous CMV episode and before the start date of the subsequent CMV episode, or if the start date of the anti-CMV was after the last CMV episode. Preemptive treatment is defined as anti-CMV treatment was initiated preemptively when the plasma CMV DNA concentration necessitated therapy based on the risk profile of the participant per clinical judgement. Percentage of participants with anti-CMV primary or secondary prophylaxis and preemptive treatment overall, at index episode and for recurrent episodes will be reported.	Up to 7 years 3 months
Secondary	Number of Anti-CMV Therapies Used for Primary or Secondary Prophylaxis and Preemptive Treatment	Primary Prophylaxis is defined as when the start date of the anti-CMV prophylaxis was prior to start date of first CMV episode. Secondary Prophylaxis is defined as when the start date of the anti-CMV prophylaxis was on/ after the end date of the previous CMV episode and before the start date of the subsequent CMV episode, or if the start date of the anti-CMV was after the last CMV episode. Preemptive treatment is defined as anti-CMV treatment was initiated preemptively when the plasma CMV DNA concentration necessitated therapy based on the risk profile of the participant per clinical judgement. Number of anti-CMV therapies used for primary or secondary prophylaxis and preemptive treatment will be reported.	Up to 7 years 3 months
Secondary	Duration of Anti-CMV Prophylaxis Therapy	Duration of anti-CMV prophylaxis therapy will be reported.	Up to 7 years 3 months
Secondary	Percentage of Participants With Mono-therapy and Dual-therapy of Anti-CMV Agents of Interest During CMV Episodes	Monotherapy of anti-CMV agents of interest includes specifically ganciclovir, valganciclovir, foscarnet, cidofovir, letermovir and maribavir, and dual therapy, namely ganciclovir and foscarnet, valganciclovir and foscarnet, cidofovir and valganciclovir, cidofovir and valganciclovir, others which includes acyclovir, valacyclovir, immunoglobulin G (IgG), etc. CMV episode is generally characterized by elevated CMV viremia levels resulting in anti-CMV treatment. Percentage of participants with mono-therapy and dual-therapy of anti-CMV agents of interest during CMV episodes will be reported.	Up to 7 years 3 months
Secondary	Number of Individual and Dual-therapy of Anti-CMV Agents Used During CMV Episodes	CMV episode is generally characterized by elevated CMV viremia levels resulting in anti-CMV treatment. Number of individual and dual-therapy of anti-CMV agents used during CMV episodes will be reported.	Up to 7 years 3 months
Secondary	Number With Individual and Dual Therapy of Anti-CMV Agents Used by Line of Treatment Overall and During the Index Episodes	Index episode is first CMV episode in which the participant is considered RRI to anti-CMV treatment or had CMV viremia and received pre-emptive treatment, without becoming RRI during that episode. Number of individual and dual therapy of anti-CMV agents used by line of treatment overall and during the index episodes will be reported.	Up to 7 years 3 months
Secondary	Duration of Anti-CMV Therapy During CMV Episodes	CMV episode is generally characterized by elevated CMV viremia levels resulting in anti-CMV treatment. Duration of anti-CMV therapy during CMV episodes will be reported.	Up to 7 years 3 months
Secondary	Number of Participants With Distribution of Switches of Anti-CMV Agents at the Index Date	Index date is the date when participant was considered resistant, refractory or intolerant to anti-CMV treatment for the first time after transplant (RRI CMV index date) or pre-emptive treatment for the first time after transplant following CMV viremia (CMV preemptive treatment index date. Number of participants with distribution of switches of anti-CMV agents at the index date will be reported.	Up to 7 years 3 months
Secondary	Percentage of Participants Administered With First, Second, Third and Fourth Line of Anti-CMV Treatments From SOT	Percentage of participants administered with first, second, third and fourth line of anti-CMV treatments from SOT will be reported.	Up to 7 years 3 months
Secondary	Time From SOT to Administration of First-line Anti-CMV Agents of Interest and Between First-line Through the Fourth Line of Treatment	Anti-CMV agents of interest includes specifically ganciclovir, valganciclovir, foscarnet, cidofovir, letermovir and maribavir, ganciclovir and foscarnet, valganciclovir and foscarnet, cidofovir and valganciclovir, cidofovir and valganciclovir, others which includes acyclovir, valacyclovir, immunoglobulin G (IgG), etc.	Up to 7 years 3 months
Secondary	Number of Participants Based on Reasons for Anti-CMV Dose Changes or Discontinuation for Anti-CMV Agents of Interest	Recurrent episodes is defined as new CMV infection in a participant with previous evidence of CMV infection. Index episode is first CMV episode in which the participant is considered RRI to anti-CMV treatment or had CMV viremia and received pre-emptive treatment, without becoming RRI during that episode. CMV episode is generally characterized by elevated CMV viremia levels resulting in anti-CMV treatment. Number of participants based on reasons for anti-CMV dose changes or discontinuation for anti-CMV agents of interest overall during CMV episodes, the index episode and for recurrent episodes will be reported.	Up to 7 years 3 months
Secondary	Number of Participants With Anti-CMV Agent Administered When Diagnosed With Myelosuppression and Nephrotoxicity	Index episode is first CMV episode in which the participant is considered RRI to anti-CMV treatment or had CMV viremia and received pre-emptive treatment, without becoming RRI during that episode. CMV episode is generally characterized by elevated CMV viremia levels resulting in anti-CMV treatment.	Up to 7 years 3 months
Secondary	Number of Participants Using Immunosuppressant From SOT	Number of participants using immunosuppressant from SOT will be reported.	Up to 7 years 3 months
Secondary	Number of Participants With CMV-related Outpatient Clinic Visits From SOT and Index Date	Index date is the date when participant was considered resistant, refractory or intolerant to anti-CMV treatment for the first time after transplant (RRI CMV index date) or pre-emptive treatment for the first time after transplant following CMV viremia (CMV preemptive treatment index date. Number of participants with CMV-related outpatient clinic visits from SOT and index date will be reported.	From SOT and index date up to 7 years 3 months
Secondary	Number of Participants Based on Selected Procedures Performed at Outpatient Clinical Visits From SOT and Index Date	Index date is the date when participant was considered resistant, refractory or intolerant to anti-CMV treatment for the first time after transplant (RRI CMV index date) or pre-emptive treatment for the first time after transplant following CMV viremia (CMV preemptive treatment index date. Selected procedures include preemptive monitoring, diagnostic imaging, treatment infusion, toxicities from anti-CMV agents.	From SOT and index date up to 7 years 3 months
Secondary	Number of Participants Based on CMV-related Hospitalizations and Emergency Department Visits From SOT and Index Date	Index date is the date when participant was considered resistant, refractory or intolerant to anti-CMV treatment for the first time after transplant (RRI CMV index date) or pre-emptive treatment for the first time after transplant following CMV viremia (CMV preemptive treatment index date. Number of participants based on CMV-related hospitalizations and emergency department visits from SOT and index date will be reported.	From SOT and index date up to 7 years 3 months
Secondary	Number of Participants Categorized Based on Reasons for CMV-related Hospitalization	Primary reason for hospitalization will include treatment infusions, CMV progression. Number of participants categorized based on reasons for CMV-related hospitalization will be reported.	Up to 7 years 3 months
Secondary	Number of Participants Based on Selected Procedures Performed at Hospitalizations and Emergency Department Visits From SOT and Index Date	Index date is the date when participant was considered resistant, refractory or intolerant to anti-CMV treatment for the first time after transplant (RRI CMV index date) or pre-emptive treatment for the first time after transplant following CMV viremia (CMV preemptive treatment index date. Selected procedures will include diagnostic imaging, treatment infusion, toxicities from anti-CMV agents.	From SOT and index date up to 7 years 3 months
Secondary	Length of Hospital Stay for CMV-related Hospitalizations and Hospital Acquired CMV Viremia	Length of hospital stay in days for CMV-related hospitalizations and hospital acquired CMV viremia will be reported.	Up to 7 years 3 months
Secondary	Duration of Stay in Critical Care and Non-critical Care	Duration in days of stay in critical care and non-critical care will be reported.	Up to 7 years 3 months

External Links

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