AspergillosisPhase 3NCT00412893
Isavuconazole (BAL8557) for Primary Treatment of Invasive Aspergillosis
A Phase 3 study testing Isavuconazole and Voriconazole in people with Aspergillosis and Invasive Fungal Infection, run by Astellas Pharma Inc at 107 sites in 26 countries.
Trial summary
The purpose of this study is to compare the efficacy and safety of isavuconazole versus voriconazole in the treatment of patients with invasive aspergillosis. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Aspergillosis, Invasive Fungal Infection
- What is being tested?
- Isavuconazole and Voriconazole
- Type of treatment
- Pill or oral medicine, Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 527 participants
- Where
- 107 sitesin 26 countries
- Study dates
- 7 Mar 2007to 28 Mar 2013
- Phase
- Phase 3
- Are there results?
- Yes, posted in the registrySummary in the doctors' view
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Patients must have proven, probable or possible invasive fungal disease caused by Aspergillus species or other filamentous fungi
- Female patients must be non-lactating and at no risk for pregnancy
Who cannot join
- Patients with invasive fungal infections other than Aspergillus species or other filamentous fungi
- Evidence of hepatic dysfunction at Baseline or moderate to severe renal dysfunction
- Patients with chronic aspergillosis, or aspergilloma or allergic bronchopulmonary aspergillosis
- Patients who have received more than 4 days of systemic antifungal therapy other than fluconazole within the 7 days prior to the first administration of study medication
- Patients previously enrolled in a Phase III study with isavuconazole
- Patients with a body weight </= 40 kg
Trial locations and contacts
107 sites in 26 countries.
107 sites in 26 countries
China12 sites
3rd Hospital, Peking University
Beijing, 100083
The 1st Hospital, Jilin University
Changchun, 130021
The Third Xiangya Hospital of Central South University
Changsha, 410013
West China Hospital of Sichuan University
Chengdu, 610041
The Affiliated Union Hospital of Fujian Medical University
Fuzhou, 350001
The First Affiliated Hospital, Med. School, Zhejiang Uni.
Hangzhou, 310003
The First Affiliated Hospital of Nanjing Medical University
Nanjing, 310009
The 1st Affiliated Hospital of Guangxi Medical University
Nanning, 530021
Huashan Hospital, Insitute of Antibiotics
Shanghai, 200040
No.6 Renmin Hosp. of Shanghai City
Shanghai, 200233
Chang Hai Hospital
Shanghai, 200433
Wuhan Union Hospital
Wuhan, 430022
United States11 sites
Upstate Infectious Diseases Association LLP
Albany, New York, 12208
University of Alabama
Birmingham, Alabama, 35294-0006
Brigham & Womens Hospital
Boston, Massachusetts, 02115
University of Chicago, Division of Infectious Diseases
Chicago, Illinois, 60637
University of Texas MD Anderson Cancer Center
Houston, Texas, 77030
Infectious Disease of Indiana
Indianapolis, Indiana, 46280
Regional Infection Diseases Infusion Center Inc.
Lima, Ohio, 45801
University of California at San Francisco
San Francisco, California, 94143
Indiana BMT
Springfield, Illinois, 62703
Springfield Clinic LLP
Springfield, Illinois, 62703
Study site
Worcester, Massachusetts, 01655
India8 sites
Sterling Hospital
Ahmedabad, Gujarat, 380052
Apollo Hospitals
Hyderabad, Andh Prad, 500033
Kasturba Medical College and Hospital
Mangalore, Karna, 575001
Shirdi Sai Baba Cancer Hospital K. M. C. Hospital
Manipal, Karna, 576104
Tata Memorial Hopital, Department of Anesthesia
Mumbai, Mahara, 400012
Study site
Noida, Uttar Prad, 201301
Deenanath Mangeshkar Hospital & Research Centre
Pune, Mahara, 411004
Sahyadri Hospital
Pune, Mahara, 411004
Argentina7 sites
Study site
Buenos Aires, C1039AAO
Study site
Buenos Aires, C1157ADP
Study site
Buenos Aires
Study site
Capital Federal, C1180AAV
Study site
Capital Federal, C1405DCS
Hospital Italiano de Buenos Aires
Ciudad Autonoma, 1181
Instituto Medico Especializado Alexander Fleming
Ciudad Autonoma, 1426
Germany7 sites
Universitaetsklinikum Aachen
Aachen, 52074
Charité Universitaetsmedizin Berlin- Campus Charité Mitte
Berlin, 12200
Universitaet Koeln
Cologne, 50937
Universitaetsklinik Leipzig
Leipzig, 04289
Study site
Lübeck, 23538
Klinikum Schwabing
München, 81737
Medizinische klinik und Polyklinik II
Würzburg, 97080
Thailand6 sites
Songklanagarind Hospital
Hat Yai, 90110
Study site
Khon Kaen, 40002
Maharat Nakhon Ratchasima Hospital
Muang, 30000
Srinagarind Hospital
Muang, 40002
Maharaj Nakorn Chiang Mai Hospital
Muang, 50200
Study site
Songkhla, 90110
Belgium5 sites
AZ ST Jan
Bruges, 8000
Institut Jules Bordet
Brussels, 1000
ULB Hospital Erasme
Brussels, 1070
Universitair Ziekenhuis Gent
Ghent, 9000
Universitaire Ziekenhuizen Leuven
Leuven, 3000
Brazil5 sites
Felicio Rocho
Belo Horizonte, 30110-908
Santa Casa de Misericordia de Belo Horizonte
Belo Horizonte, 30150-221
Hospital das Clinicas da UFPR
Curitiba, 80060-150
Hospital de Clinicas da FMUSP - Ribeirao Preto
Ribeirão Preto, 14048-900
Hospital Universitario Clementino Fraga Filho
Rio de Janeiro, 21941-913
France5 sites
Study site
Dijon, 21079
CHU de Nantes - Hôpital Hôtel Dieu
Nantes, 44035
Hotel Dieu
Nantes, 44093
Hôpital Hautepierre
Strasbourg, 67098
Hôpital de brabois adultes
Vandœuvre-lès-Nancy, 54511
Israel5 sites
Rambam Health Care Campus
Haifa, 31096
Hadassah Universtiy Hospital - Ein Kerem
Jerusalem, 91200
Rabin MC
Petah Tikva, 49100
Chaim Sheba Medical Center
Ramat Gan, 52621
Sourasky MC Ichilov Hospital Tel Aviv
Tel Aviv, 64239
Russia5 sites
State Institution "Hematology Research Center" RAMS
Moscow, 125167
Republican Hospital named after V.A. Baranov
Petrozavodsk, 185019
Leningrad Regional Hospital
Saint Petersburg, 194291
St-Petersburg MA Postgraduate Education
Saint Petersburg, 194291
Study site
Saint Petersburg, 197089
South Korea5 sites
Gachon University Gil Hospital
Incheon, 405-760
Study site
Seoul, 120-752
Samsung Medical Center
Seoul, 135-710
The Catholic University of Korea, St. Mary's Hospital
Seoul, 137-701
Asan Medical Center
Seoul, 138-736
Australia3 sites
Study site
Perth, 6000
Mater Medical Centre
South Brisbane, 4101
Study site
Woolloongabba, 4102
Chile3 sites
Study site
Santiago
Hospital Dr. Hernan Henriquez Aravena
Temuco, 4780000
Study site
Valdivia, 5090000
Egypt3 sites
Alexandria University Hospital
Alexandria, 21131
National Cancer Institute
Cairo, 11796
Nasser Institute
Cairo, 12655
Hungary3 sites
Study site
Budapest, 1094
Petz Aladar Megyei Oktato Korhaz
Győr, 9024
Szegedi Tudomanyegyetem
Szeged, 6720
Canada2 sites
Hamilton Health Sciences - Henderson Site
Hamilton, L8V 1C3
The Ottawa Hospital - General Campus
Ottawa, Ontario, K1H 8L6
Italy2 sites
Unità Funzionale di Ematologia; Azienda Ospedaliera Universitaria Careggi
Florence, 50134
Azienda Ospedaliera Ospedale Niguarda Ca' Granda
Milan, 20162
Mexico2 sites
Study site
México, 06726
Hospital Universitario Dr Jose Eleuterio Gonzalez
Monterrey, 64040
About this study
Official title: A Phase III, Double Blind, Randomized Study to Evaluate Safety and Efficacy of BAL8557 Versus Voriconazole for Primary Treatment of Invasive Fungal Disease Caused by Aspergillus Species or Other Filamentous Fungi.
The purpose of this study is to compare the efficacy and safety of isavuconazole versus voriconazole in the treatment of patients with invasive aspergillosis.
Read the detailed description
Acute invasive fungal infections caused by aspergillus, zygomycetes and other filamentous fungi remain life threatening diseases. Early treatment with highly effective anti-fungals reduces mortality. This study investigates the efficacy and safety of isavuconazole in the treatment of invasive fungal diseases, caused by Aspergillus or other filamentous fungi.
- Conditions
- Aspergillosis, Invasive Fungal Infection
- Being tested
- Isavuconazole, Voriconazole
- Keywords
- Invasive fungal disease, BAL8557, Isavuconazole, ASP9766, Filamentous fungi, Phase III, Aspergillus species
- Medical subject headings
- Aspergillosis, Invasive Fungal Infections
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
IsavuconazoleDrug
Also called ASP9766, BAL8557
Loading doses were administered as IV infusion and maintenance doses were administered as IV infusion or oral (capsules).
VoriconazoleDrug
Also called VFend
Loading doses were administered as IV infusion and maintenance doses were administered as IV infusion or oral (capsules).
| Study group | Role | What they receive |
|---|---|---|
| Isavuconazole | Experimental | Participants received a loading dose of isavuconazole, 200 mg three times a day by intravenous infusion (IV) for the first 2 days followed by a maintenance dose from Day 3 of 200 mg once daily either IV or orally until they reached a treatment endpoint or for a maximum of 84 days. Receives: Drug: Isavuconazole |
| Voriconazole | Active comparator | Participants received a loading dose of voriconazole, 6 mg/kg every 12 hours IV for the first 24 hours, followed by a maintenance dose of 4 mg/kg every 12 hours by IV on Day 2. Beginning on Day 3, participants received 4 mg/kg every 12 hours by IV or 200 mg every 12 hours orally, until they reached a treatment endpoint or for a maximum of 84 days. Receives: Drug: Voriconazole |
What is being measured
The primary outcome is the main question the study is designed to answer.
All-cause Mortality Through Day 42
All-cause mortality is represented as the percentage of participants who died after first dose of study drug through Day 42 from any cause. Participants with unknown survival status through Day 42 were included as deaths in the calculation.
Measured: Through Day 42
Secondary outcomes (10)
Percentage of Participants With an Overall Outcome of Success Evaluated by the Data Review Committee (DRC)
The DRC was an independent, blinded committee consisting of experts in the field of infectious disease who assessed patients' outcomes. The overall response was based on the DRC-assessed clinical, mycological and radiological responses. Success was defined as the resolution or partial resolution of all attributable clinical symptoms and physical findings, the eradication or presumed eradication of the original causative organism cultured or identified by histology/cytology at Baseline and a > 50% improvement in radiological response from Baseline (or improvement of at least 25% from Baseline for the Day 42 analysis or End of Treatment if it occurred prior to Day 42). End of treatment (EOT) is the last day of study drug administration. For the Day 42 and Day 84 analyses, any visits that the DRC assessed as Not Done were considered a failure for that visit. A death before Day 42 was also considered a failure, even if the DRC assessed the participant to be a success prior to death.
Measured: Day 42, Day 84 and End of Treatment. The median duration of study drug administration was 45 days.
All-cause Mortality Through Day 84
All-cause mortality is represented as the percentage of participants who died after first dose of study drug through Day 84 from any cause. Participants with unknown survival status through Day 84 were included as deaths in the calculation.
Measured: Through Day 84
Percentage of Participants With an Overall Outcome of Success Evaluated by Investigator
Overall response based on investigators' assessments was not derived as it was not deemed necessary because participants overall response status was determined by the DRC. All investigators' assessments of clinical, mycological and radiological responses are analyzed separately (see Outcome Measures 8-10).
Measured: Day 42, Day 84 and End of Treatment. The median duration of study drug administration was 45 days.
Percentage of Participants With a Clinical Response Assessed by the DRC
Blinded assessments of clinical symptoms and physical findings of invasive fungal disease were performed by the independent DRC. Clinical response is defined as the resolution or partial resolution of all attributable clinical symptoms and physical findings. Failure is defined as no resolution of any attributable clinical symptoms and physical findings and/or worsening. Participants with no attributable signs and symptoms present at Baseline and no symptoms attributable to invasive fungal disease (IFD) developed post-baseline were classified as "Not Applicable." End of treatment is the last day of study drug administration.
Measured: Day 42, Day 84 and End of Treatment. The median duration of study drug administration was 45 days.
Percentage of Participants With a Mycological Response Assessed by the DRC
Blinded mycological assessments of the participant's invasive fungal disease status were performed by the independent DRC using the results from fungal culture and isolation and/or histology/cytology of biopsy or biological fluid samples from the infected site. Mycological response is defined as eradication or presumed eradication of the original causative organism cultured or identified by histology/cytology at Baseline. Failure was defined as persistence or presumed persistence. Participants with no mycological evidence available at Baseline were classified as "Not Applicable". End of treatment is the last day of study drug administration.
Measured: Day 42, Day 84 and End of Treatment. The median duration of study drug administration was 45 days.
Percentage of Participants With a Radiological Response Assessed by the DRC
Independent reviews of radiology assessments were completed by radiology experts which were provided to the independent, blinded DRC. Blinded radiological assessments were performed by the DRC. Radiological response is defined as a ≥ 50% improvement from Baseline, or improvement of at least 25% from Baseline for the Day 42 analysis or if end of treatment occurred before Day 42. Participants without any radiology at Baseline were considered "Not Applicable." End of Treatment is the last day of study drug administration.
Measured: Day 42, Day 84 and End of Treatment. The median duration of study drug administration was 45 days.
Percentage of Participants With a Clinical Response Assessed by the Investigator
Assessment of clinical symptoms and physical findings of invasive fungal disease were performed by the investigator. Clinical response is defined as the resolution or partial resolution of all attributable clinical symptoms and physical findings. Failure is defined as no resolution of any attributable clinical symptoms and physical findings and/or worsening, or if results were unavailable or the participant was unevaluable. Participants with no attributable signs and symptoms present at Baseline were classified as "Not Applicable." End of treatment is the last day of study drug administration.
Measured: Day 42, Day 84 and End of Treatment. The median duration of study drug administration was 45 days.
Percentage of Participants With a Mycological Response Assessed by the Investigator
Mycological assessments of the participant's invasive fungal disease status were performed by the investigator using the results from fungal culture and isolation and/or histology/cytology of biopsy or biological fluid samples from the infected site. Mycological response is defined as eradication or presumed eradication of the original causative organism cultured or identified by histology/cytology at Baseline. Failure was defined as persistence or presumed persistence. Participants with no mycological evidence available at Baseline, or no mycological follow-up results available or indeterminate results were classified as "Not Applicable". End of treatment is the last day of study drug administration.
Measured: Day 42, Day 84 and End of Treatment. The median duration of study drug administration was 45 days.
Percentage of Participants With a Radiological Response Assessed by the Investigator
Radiological assessments were performed by the investigator. Radiological response is defined as a ≥ 50% improvement from Baseline, or improvement of at least 25% from Baseline for the Day 42 analysis or if end of treatment occurred before Day 42. Failure is defined as a < 25% improvement at any time or results not available. Participants with no signs on radiological images at Baseline were considered "Not Applicable." End of Treatment is the last day of study drug administration.
Measured: Day 42, Day 84 and End of Treatment. The median duration of study drug administration was 45 days.
Number of Participants With Adverse Events, Reported by System Organ Class
Measured: From the first study drug administration until 28 days after the last dose of study drug. The median duration of study drug administration was 45 days.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted19 Dec 2006 (estimated)
- Study start7 Mar 2007
- Primary completion28 Mar 2013
- Study completion28 Mar 2013
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Publications (3)Papers the sponsor has linked to this study.
- Other trials for AspergillosisStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 3
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind
- Who is masked
- Participant, Investigator
- Enrolment
- 527 participants (actual)
Sponsor and investigators
- Lead sponsor
- Astellas Pharma Inc
- Sponsor type
- Industry (pharma, biotech, devices)
- Collaborators
- Basilea Pharmaceutica International Ltd
- Responsible party
- Sponsor
- Investigators
- Medical Director, Study director, Astellas Pharma Global Development
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00412893
- Sponsor's protocol ID
- 9766-CL-0104
- Other IDs
- WSA-CS-004, 2006-003868-59
- Status last verified
- Nov 2024
- First submitted
- 18 Dec 2006
- Last updated
- 10 Dec 2024
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- Yes
- Individual data sharing
- Yes: Access to anonymized individual participant level data collected during the study, in addition to study-related supporting documentation, is planned for studies conducted with approved product indications and formulations, as well as products terminated during development. Studies conducted with product indications or formulations that remain active in development are assessed after study completion to determine if Individual Participant Data can be shared. Further details on Astellas' data sharing policy can be found at https://www.clinicaltrials.astellas.com/transparency/.
Publications
Hamed K, Engelhardt M, Kovanda LL, Huang JJ, Yan J, Aram JA. Post-hoc analysis of the safety and efficacy of isavuconazole in older patients with invasive fungal disease from the VITAL and SECURE studies. Sci Rep. 2023 Apr 25;13(1):6730. doi: 10.1038/s41598-023-31788-1.
PubMed 37185921Kovanda LL, Kolamunnage-Dona R, Neely M, Maertens J, Lee M, Hope WW. Pharmacodynamics of Isavuconazole for Invasive Mold Disease: Role of Galactomannan for Real-Time Monitoring of Therapeutic Response. Clin Infect Dis. 2017 Jun 1;64(11):1557-1563. doi: 10.1093/cid/cix198.
PubMed 28472247Maertens JA, Raad II, Marr KA, Patterson TF, Kontoyiannis DP, Cornely OA, Bow EJ, Rahav G, Neofytos D, Aoun M, Baddley JW, Giladi M, Heinz WJ, Herbrecht R, Hope W, Karthaus M, Lee DG, Lortholary O, Morrison VA, Oren I, Selleslag D, Shoham S, Thompson GR 3rd, Lee M, Maher RM, Schmitt-Hoffmann AH, Zeiher B, Ullmann AJ. Isavuconazole versus voriconazole for primary treatment of invasive mould disease caused by Aspergillus and other filamentous fungi (SECURE): a phase 3, randomised-controlled, non-inferiority trial. Lancet. 2016 Feb 20;387(10020):760-9. doi: 10.1016/S0140-6736(15)01159-9. Epub 2015 Dec 10.
PubMed 26684607
Study at a glance
From the registry record, last updated by the sponsor on 10 Dec 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Phase III, Double Blind, Randomized Study to Evaluate Safety and Efficacy of BAL8557 Versus Voriconazole for Primary Treatment of Invasive Fungal Disease Caused by Aspergillus Species or Other Filamentous Fungi.
- ClinicalTrials.gov ID
- NCT00412893
- Acronym / sponsor ID
- 9766-CL-0104
- Conditions
- Aspergillosis, Invasive Fungal Infection
- Keywords
- Invasive fungal disease, BAL8557, Isavuconazole, ASP9766, Filamentous fungi, Phase III, Aspergillus species
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 527 participants (actual)
- Lead sponsor
- Astellas Pharma IncIndustry (pharma, biotech, devices)
- Collaborators
- Basilea Pharmaceutica International Ltd
- Study start
- 7 Mar 2007 (actual)
- Primary completion
- 28 Mar 2013 (actual)
- Study completion
- 28 Mar 2013 (actual)
- First posted
- 19 Dec 2006 (estimated)
- Results
- Posted 31 Mar 2015
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The purpose of this study is to compare the efficacy and safety of isavuconazole versus voriconazole in the treatment of patients with invasive aspergillosis.
Detailed description
Acute invasive fungal infections caused by aspergillus, zygomycetes and other filamentous fungi remain life threatening diseases. Early treatment with highly effective anti-fungals reduces mortality. This study investigates the efficacy and safety of isavuconazole in the treatment of invasive fungal diseases, caused by Aspergillus or other filamentous fungi.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, investigator)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Isavuconazole | Experimental | Drug: IsavuconazoleParticipants received a loading dose of isavuconazole, 200 mg three times a day by intravenous infusion (IV) for the first 2 days followed by a maintenance dose from Day 3 of 200 mg once daily either IV or orally until they reached a treatment endpoint or for a maximum of 84 days. |
| Voriconazole | Active comparator | Drug: VoriconazoleParticipants received a loading dose of voriconazole, 6 mg/kg every 12 hours IV for the first 24 hours, followed by a maintenance dose of 4 mg/kg every 12 hours by IV on Day 2. Beginning on Day 3, participants received 4 mg/kg every 12 hours by IV or 200 mg every 12 hours orally, until they reached a treatment endpoint or for a maximum of 84 days. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (2 listed)
- Patients must have proven, probable or possible invasive fungal disease caused by Aspergillus species or other filamentous fungi
- Female patients must be non-lactating and at no risk for pregnancy
Key exclusion criteria (6 listed)
- Patients with invasive fungal infections other than Aspergillus species or other filamentous fungi
- Evidence of hepatic dysfunction at Baseline or moderate to severe renal dysfunction
- Patients with chronic aspergillosis, or aspergilloma or allergic bronchopulmonary aspergillosis
- Patients who have received more than 4 days of systemic antifungal therapy other than fluconazole within the 7 days prior to the first administration of study medication
- Patients previously enrolled in a Phase III study with isavuconazole
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| IsavuconazoleAlso: ASP9766, BAL8557Loading doses were administered as IV infusion and maintenance doses were administered as IV infusion or oral (capsules). | Drug | Isavuconazole |
| VoriconazoleAlso: VFendLoading doses were administered as IV infusion and maintenance doses were administered as IV infusion or oral (capsules). | Drug | Voriconazole |
Primary outcome
All-cause Mortality Through Day 42
Time frame: Through Day 42
All-cause mortality is represented as the percentage of participants who died after first dose of study drug through Day 42 from any cause. Participants with unknown survival status through Day 42 were included as deaths in the calculation.
10 secondary outcomes
Percentage of Participants With an Overall Outcome of Success Evaluated by the Data Review Committee (DRC)
Time frame: Day 42, Day 84 and End of Treatment. The median duration of study drug administration was 45 days.
All-cause Mortality Through Day 84
Time frame: Through Day 84
Percentage of Participants With an Overall Outcome of Success Evaluated by Investigator
Time frame: Day 42, Day 84 and End of Treatment. The median duration of study drug administration was 45 days.
Percentage of Participants With a Clinical Response Assessed by the DRC
Time frame: Day 42, Day 84 and End of Treatment. The median duration of study drug administration was 45 days.
Percentage of Participants With a Mycological Response Assessed by the DRC
Time frame: Day 42, Day 84 and End of Treatment. The median duration of study drug administration was 45 days.
Percentage of Participants With a Radiological Response Assessed by the DRC
Time frame: Day 42, Day 84 and End of Treatment. The median duration of study drug administration was 45 days.
Percentage of Participants With a Clinical Response Assessed by the Investigator
Time frame: Day 42, Day 84 and End of Treatment. The median duration of study drug administration was 45 days.
Percentage of Participants With a Mycological Response Assessed by the Investigator
Time frame: Day 42, Day 84 and End of Treatment. The median duration of study drug administration was 45 days.
Percentage of Participants With a Radiological Response Assessed by the Investigator
Time frame: Day 42, Day 84 and End of Treatment. The median duration of study drug administration was 45 days.
Number of Participants With Adverse Events, Reported by System Organ Class
Time frame: From the first study drug administration until 28 days after the last dose of study drug. The median duration of study drug administration was 45 days.
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 10 Dec 2024.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Derived from this study: PubMed 37185921Hamed K, Engelhardt M, Kovanda LL, Huang JJ, Yan J, Aram JA. Post-hoc analysis of the safety and efficacy of isavuconazole in older patients with invasive fungal disease from the VITAL and SECURE studies. Sci Rep. 2023 Apr 25;13(1):6730. doi: 10.1038/s41598-023-31788-1.
- Derived from this study: PubMed 28472247Kovanda LL, Kolamunnage-Dona R, Neely M, Maertens J, Lee M, Hope WW. Pharmacodynamics of Isavuconazole for Invasive Mold Disease: Role of Galactomannan for Real-Time Monitoring of Therapeutic Response. Clin Infect Dis. 2017 Jun 1;64(11):1557-1563. doi: 10.1093/cid/cix198.
- Derived from this study: PubMed 26684607Maertens JA, Raad II, Marr KA, Patterson TF, Kontoyiannis DP, Cornely OA, Bow EJ, Rahav G, Neofytos D, Aoun M, Baddley JW, Giladi M, Heinz WJ, Herbrecht R, Hope W, Karthaus M, Lee DG, Lortholary O, Morrison VA, Oren I, Selleslag D, Shoham S, Thompson GR 3rd, Lee M, Maher RM, Schmitt-Hoffmann AH, Zeiher B, Ullmann AJ. Isavuconazole versus voriconazole for primary treatment of invasive mould disease caused by Aspergillus and other filamentous fungi (SECURE): a phase 3, randomised-controlled, non-inferiority trial. Lancet. 2016 Feb 20;387(10020):760-9. doi: 10.1016/S0140-6736(15)01159-9. Epub 2015 Dec 10.
- Individual participant dataSharing planned: Yes. Access to anonymized individual participant level data collected during the study, in addition to study-related supporting documentation, is planned for studies conducted with approved product indications and formulations, as well as products terminated during development. Studies conducted with product indications or formulations that remain active in development are assessed after study completion to determine if Individual Participant Data can be shared. Further details on Astellas' data sharing policy can be found at https://www.clinicaltrials.astellas.com/transparency/.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Medical Director study director
Astellas Pharma Global Development
107 sites in 26 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing Isavuconazole and Voriconazole in people with Aspergillosis and Invasive Fungal Infection, run by Astellas Pharma Inc at 107 sites in 26 countries.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 10 Dec 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 107 sites in China, United States, India, Argentina, Germany and 21 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
Yes. Results are posted in the registry (first posted 31 Mar 2015). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
All-cause Mortality Through Day 42 (time frame: Through Day 42). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT00412893, which also lists 3 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Dec 2024.