Hepatocellular CarcinomaPhase 3YES-PNCT01887717
Efficacy Evaluation of TheraSphere to Treat Inoperable Liver Cancer With Blockage of the Portal Vein
A Phase 3 study testing TheraSphere® and Sorafenib in people with Hepatocellular Carcinoma, run by Boston Scientific Corporation at 19 sites in 6 countries.
Trial summary
This is a two-arm, open-label, prospective, multi-center, randomized, active-controlled clinical trial to assess efficacy and safety of TheraSphere in comparison to standard of care therapy (sorafenib) in the treatment of participants with inoperable liver cancer and blockage of the portal vein. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Hepatocellular Carcinoma
- What is being tested?
- TheraSphere® and Sorafenib
- Type of treatment
- Pill or oral medicine, Medical device
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 36 participants
- Where
- 19 sitesin 6 countries
- Study dates
- 27 Feb 2014to 23 May 2017
- 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
- Participants over 18 years of age, regardless of race or gender
- Advanced unresectable hepatocellular carcinoma with branch portal vein thrombosis (confirmed by non-invasive criteria European Association for the Study of the Liver [EASL]/American Association for the Study of Liver Diseases [AASLD], mandatory by histology in non-cirrhotic participants); can be naive or recurrent HCC after curative treatment ( >6 months before randomization)
- Unilobar disease
- Child Pugh A
- Tumor volume ≤70% of liver volume (determined by visual estimation)
- At least one uni-dimensional HCC target lesion assessable by computed tomography (CT) or magnetic resonance imaging (MRI) according to Response Evaluation Criteria in Solid Tumor (RECIST) version 1.1
Show all 13Show fewer
- Eastern Cooperative Oncology Group (ECOG) Performance Status 0-1
- Platelets ≥ 50*10^3/microliter (µL)
- White blood cell (WBC) ≥1.5*10^3/microliter (µL)
- Aspartate transaminase (AST)/ alanine aminotransferase (ALT) ≤5 times upper limit of normal
- Creatinine ≤2.0 mg/deciliter (dL)
- Life expectancy >3 months
- Signed informed consent
Who cannot join
- Confirmed extra hepatic metastases. Participants with indeterminate hepatic hilar lymph nodes up to 2.5 centimeters (cm) in greatest dimension, or with indeterminate lung nodules (single lesion between 1-1.5 cm, or multiple smaller lesions with a total diameter of ≤2 cm) may be included if metastatic disease is deemed unlikely
- Known contraindication to standard-of-care sorafenib including allergic reaction, pill swallowing difficulty, uncontrolled hypertension or history of cardiac disease, significant GI bleed within 30 days, and renal failure including dialysis
- Evidence of hepatic vein invasion or caval thrombosis
- Evidence of chronic obstructive pulmonary disease
- Indication for any possible curative treatment after multidisciplinary assessment (surgery, ablation, transplantation)
- Previous treatment with sorafenib for more than 4 weeks during the previous 2 months; prior sorafenib-related toxicity
Show all 18Show fewer
- Initiation of anti-tumor therapy including chemotherapy or investigational drug treatment within 30 days before beginning study
- Prior transarterial chemoembolization (TACE) <6 months prior to screening phase in case of participants progressing from an intermediate to an advanced stage due to occurrence of PVT
- On a transplant list
- History of organ allograft
- Contraindications to angiography or selective visceral catheterization
- History of severe allergy or intolerance to contrast agents, narcotics, sedatives, or atropine that cannot be managed medically
- Prior external beam radiation therapy to the liver
- Evidence of continuing adverse effect of prior therapy
- Active gastrointestinal (GI) bleeding and any bleeding diathesis or coagulopathy that is not correctable by usual therapy or hemostatic agents
- Evidence of any disease or condition that would place the participant at undue risk and preclude safe use of TheraSphere treatment
- Females of child-bearing potential must have a negative serum test
- No participation in concurrent clinical trials
Trial locations and contacts
19 sites in 6 countries.
19 sites in 6 countries
Italy9 sites
UO Radiologia, Ospedali Riuniti di Bergamo
Bergamo, 24128
Azienda Ospedaliero-Universitaria di Bologna
Bologna, 40138
ASO-Santa Croce e Carle di Cuneo
Cuneo, 12100
Fondazione IRCCS Ca Grande
Milan, 20122
S.C Radiologia Interventistica, A.O.Ospedale Niguarda Ca Granda
Milan, 20162
Fondazione Istituto Nazionale Tumori di Milano
Milan, I-20133
Azienda Ospedaliera Ospedali Riuniti "Villa Sofia-Cervello"
Palermo, 90147
University of Pisa
Pisa, 56100
Policlinico A. Gemelli
Rome, 8 - 00168
Spain4 sites
Hospital Clínic Barcelona. IDIBAPS. CIBEREHD. Liver Unit
Barcelona, 08036
Bulevar Sur s/n
Madrid, 28041
Hospital Universitario Puerta de Hierro, Gastroenterology & Hepatology Dept
Madrid, 28222
Hospital Universitari i Politecnic la Fe
Valencia, 46026
United States2 sites
Northwestern Medical Faculty Foundation, Div of Hematology/Oncology
Chicago, Illinois, 60611
Mount Sinai School of Medicine
New York, New York, 10029
United Kingdom2 sites
University Hospitals Birmingham NHS Foundation Trust
Birmingham, B15 2WB
Royal Free London NHS Foundation Trust
London, NW3 2QG
About this study
Official title: A Prospective Randomized Clinical Trial on 90Yttrium Trans-arterial Radio-Embolization (TheraSphere®) vs. Standard of Care (Sorafenib) for the Treatment of Advanced Hepatocellular Carcinoma (HCC) With Portal Vein Thrombosis (PVT)
This is a two-arm, open-label, prospective, multi-center, randomized, active-controlled clinical trial to assess efficacy and safety of TheraSphere in comparison to standard of care therapy (sorafenib) in the treatment of participants with inoperable liver cancer and blockage of the portal vein.
Read the detailed description
The objective of this Phase III, prospective randomized trial is to determine whether TheraSphere provides a meaningful benefit in survival in comparison with the standard of care (sorafenib) in participants with good hepatic function and advanced hepatocellular carcinoma (HCC) associated with portal vein thrombosis (PVT).
This is an open-label prospective, multi-center, randomized, controlled clinical trial that will evaluate the use of TheraSphere compared to standard-of-care sorafenib alone.
- Conditions
- Hepatocellular Carcinoma
- Being tested
- TheraSphere®, Sorafenib
- Keywords
- hepatocellular carcinoma, portal vein thrombosis
- Medical subject headings
- Carcinoma, Hepatocellular
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
TheraSphere®Device
Also called yttrium-90 microspheres
Intrahepatic treatment of advanced hepatocellular carcinoma
SorafenibDrug
Also called Nexavar®
Standard of care therapy for treatment of advanced hepatocellular carcinoma
| Study group | Role | What they receive |
|---|---|---|
| TheraSphere | Experimental | Participants will receive TheraSphere at a dose consistent with the approved product label to the treated lobe of the liver. TheraSphere will be administered through the hepatic artery. The target dose will be 120 Gy + 10%. Dose reduction to a minimum dose of 80 Gy + 10% will be permitted to manage radiation exposure to the lungs. Re-treatment of the same participant/lobe with further cycles of TheraSphere will be permitted if a treatable progression is detected during follow-up evaluations. Any re-treatment will take place at least 28 days after the previous TheraSphere treatment administered to that lobe. Participants can receive a subsequent TheraSphere administration in the absence of radiological progression criteria at the Investigator's discretion. A maximum of 3 TheraSphere administrations will be permitted. Receives: Device: TheraSphere® |
| Sorafenib | Active comparator | Participants will receive sorafenib, oral tablets, 400 milligrams (mg) twice daily in accordance with the package insert. Treatment is to continue until the participant is no longer clinically benefiting from therapy or until unacceptable toxicity occurs. Medically appropriate dose adjustments and drug holidays due to adverse events (AEs) and toxicity will be allowed. Receives: Drug: Sorafenib |
What is being measured
The primary outcome is the main question the study is designed to answer.
Overall Survival (OS) From Time of Randomization
OS was calculated as the interval between the randomization date and the date of death for any cause, with censoring at the date of last contact for participants alive.
Measured: Randomization up to participant's death (maximum time = up to Month 30)
Secondary outcomes (7)
Time to Progression (TTP)
TTP was defined as the time from randomization until date of first radiological progression (including new liver lesions and extra-hepatic lesions) separately according to Response Evaluation Criteria in Solid Tumor (RECIST) version 1.1 criteria, modified RECIST (mRECIST) criteria, and European Association for the Study of the Liver (EASL) criteria (assessed bi-dimensionally on enhancing tissue) as assessed by Investigator determination. Progression was defined as an increase >25% in the size of ≥1 measurable lesions (EASL) and ≥20% increase in the sum of the diameter of viable of target lesion (mRECIST). RECIST v1.1 categorized new lesions as Progressive Disease. TTP (Months)=(Date of event/censor - Date of Randomization + 1)/ 30.4375.
Measured: Randomization up to participant's death (maximum time = up to Month 30)
Time to Worsening Portal Vein Thrombosis (PVT)
Time of randomization to time of any change in classification of PVT type by ≥1 sub-type based on Investigator assessment. At screening and every 8 weeks after, PVT categorized based on dynamic imaging studies as: Type I: segmental, in ≥1 of 8 branches of the portal vein; Type II: branched, left or right branches of the portal vein; Type III: modified on the basis of extension of the tumor thrombus; Type IIIa: eligible for study, thrombus involving the main trunk, allowing blood flow to contralateral lobe (no thrombosis); Type IIIb: NOT eligible for study, thrombus in the main portal trunk occluding blood flow to contralateral lobe; and Type IV: main PVT, NOT eligible for study, extended (mesenteric or splenic veins and/or sovra-hepatic veins). Time to Worsening of PVT (Months)=(Date of event/censor-Date of Randomization+1)/30.4375. Median time to event defined as time it is expected for half of the participants to experience the event. Data analyzed using the Kaplan-Meier method.
Measured: Baseline (Randomization) up to participant's death (maximum time = up to Month 30)
Time to Symptomatic Progression (TTSP)
TTSP calculated as interval between randomization and symptomatic progression. Symptomatic progression defined as clinical progress to Eastern Cooperative Oncology Group (ECOG) performance status (PS) ≥2 with or without tumor progression on imaging. Deterioration in PS was confirmed at the evaluation 8 weeks later. First date at which ECOG performance status was ≥2 was used as end date in TTSP analysis (assuming next subsequent visit confirmed deterioration). TTSP (Months)=(Date of ECOG >2-Date of Randomization+1)/30.4375. ECOG PS Scale: 0=Asymptomatic and fully active; 1=Symptomatic, fully ambulatory, restricted in physically strenuous activity; 2=Symptomatic, ambulatory, capable of self-care, more than 50% of waking hours are spent out of bed; 4=Completely disabled, no self-care, bedridden. Median time to event defined as time it is expected for half of the participants to experience the event. Data analyzed using the Kaplan-Meier method.
Measured: Randomization up to participant's death (maximum time = up to Month 30)
Number of Participants With Tumor Response
Tumor Response was based on the radiological tumor assessment and was categorized as Complete Response (CR), Partial Response (PR), Stable Disease (SD) or Progressive Disease (PD). Tumor response was assessed using RECIST version (v) 1.1, mRECIST, and EASL criteria. Criteria included: CR=disappearance of all enhanced tumor areas (EASL) and disappearance of any intratumoral arterial enhancement in all target lesions (mRECIST); PR= decrease >50% of enhanced areas (EASL) and ≥30% decrease in the sum of diameters of viable target lesions (mRECIST); SD=neither CR, PR, PD (EASL/mRECIST); PD=an increase >25% in the size of ≥1 measurable lesions (EASL) and ≥20% increase in the sum of the diameter of viable of target lesion (mRECIST). RECIST v 1.1 categorized new lesions as Progressive Disease only and the non-target lesions needed to have no progressive disease to be categorized as CR or PR. One month=30.4375 days.
Measured: Baseline up to participant's death (maximum time = up to Month 30)
Change From Baseline in Quality of Life (QoL) as Assessed by the FACT-Hep Questionnaire
The Functional Assessment Cancer of Therapy-Hepatobiliary (FACT-Hep) Questionnaire uses participant reported outcome (PRO) scores. The FACT-Hep Trial Outcome Index (TOI) is the sum of the subscales scores in Personal Well-Being (PWB), Functional Well-Being (FWB), and Hepatobiliary Cancer Subscale (HCS). The higher the score, the better the QoL, with a range 0-128. Baseline data and change from Baseline data is presented.
Measured: Baseline (Randomization), participant's death (maximum time = up to Month 30)
Time to Deterioration QoL (TTDQoL)
TTDQoL was calculated as the interval between the randomization date and deterioration in QoL. The FACT-Hep Questionnaire uses PRO scores. A deterioration in QoL is defined as a >7-point decline in the total score or death, whichever occurred first. The FACT-Hep Total Score is the sum of the subscales scores in PWB, Social/Family Well-Being (SWB), Emotional Well-Being (EWB), FWB, and HCS. The higher the score, the better the QoL, with a range 0-180. TTDQoL (Months)=(Date of change from baseline in FACT-Hep ≥7 or death) - Date of Randomization + 1.
Measured: Baseline (Randomization) up to participant's death (maximum time = up to Month 30)
Number of Participants With Treatment Emergent Adverse Events (TEAE)
An TEAE is any untoward medical occurrence or undesirable event(s) experienced in a participant that begins or worsens following administration of the study drug or study treatment, whether or not considered related to the treatment by the Investigator. A serious adverse event (SAE) was an adverse event (AE) resulting in any of the following outcomes or deemed significant for any other reason, death, initial or prolonged inpatient hospitalization, life-threatening experience (immediate risk of dying), persistent or significant disability/incapacity, or congenital anomaly. AEs included both SAEs and non-serious AEs. AEs were classified according to National Cancer Institute Common Terminology Criteria for Adverse Events v4.0 (CTCAE) and coded using the Medical Dictionary for Regulatory Activities (MedDRA). A summary of serious and all other non-serious adverse events, regardless of causality, is located in the Reported Adverse Events module.
Measured: Randomization up to participant's death (maximum time = up to Month 30)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted27 Jun 2013 (estimated)
- Study start27 Feb 2014
- Primary completion23 May 2017
- Study completion23 May 2017
Why it stopped: Poor Accrual.
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.
- Other trials for Hepatocellular CarcinomaStudies of the same condition, open and under way.
- More trials run by Boston Scientific CorporationThe sponsor's other registered studies.
- 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
- None (open label)
- Enrolment
- 36 participants (actual)
Sponsor and investigators
- Lead sponsor
- Boston Scientific Corporation
- Sponsor type
- Industry (pharma, biotech, devices)
- Collaborators
- Biocompatibles UK Ltd
- Responsible party
- Sponsor
- Investigators
- Vincenzo Mazzaferro, MD, Principal investigator, Istituto Tumori Nazionale, Milan, ItalyRiad Salem, MD, Principal investigator, Northwestern University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01887717
- Sponsor's protocol ID
- TS-104
- Other IDs
- 2012-005375-14
- Acronym
- YES-P
- Status last verified
- Apr 2021
- First submitted
- 3 Jun 2013
- Last updated
- 21 Apr 2021
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- Yes
Study at a glance
From the registry record, last updated by the sponsor on 21 Apr 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Prospective Randomized Clinical Trial on 90Yttrium Trans-arterial Radio-Embolization (TheraSphere®) vs. Standard of Care (Sorafenib) for the Treatment of Advanced Hepatocellular Carcinoma (HCC) With Portal Vein Thrombosis (PVT)
- ClinicalTrials.gov ID
- NCT01887717
- Acronym / sponsor ID
- YES-P / TS-104
- Conditions
- Hepatocellular Carcinoma
- Keywords
- hepatocellular carcinoma, portal vein thrombosis
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- TerminatedReason stopped: Poor Accrual.
- Enrolment
- 36 participants (actual)
- Lead sponsor
- Boston Scientific CorporationIndustry (pharma, biotech, devices)
- Collaborators
- Biocompatibles UK Ltd
- Study start
- 27 Feb 2014 (actual)
- Primary completion
- 23 May 2017 (actual)
- Study completion
- 23 May 2017 (actual)
- First posted
- 27 Jun 2013 (estimated)
- Results
- Posted 29 Oct 2019
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This is a two-arm, open-label, prospective, multi-center, randomized, active-controlled clinical trial to assess efficacy and safety of TheraSphere in comparison to standard of care therapy (sorafenib) in the treatment of participants with inoperable liver cancer and blockage of the portal vein.
Detailed description
The objective of this Phase III, prospective randomized trial is to determine whether TheraSphere provides a meaningful benefit in survival in comparison with the standard of care (sorafenib) in participants with good hepatic function and advanced hepatocellular carcinoma (HCC) associated with portal vein thrombosis (PVT).
This is an open-label prospective, multi-center, randomized, controlled clinical trial that will evaluate the use of TheraSphere compared to standard-of-care sorafenib alone.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| TheraSphere | Experimental | Device: TheraSphere®Participants will receive TheraSphere at a dose consistent with the approved product label to the treated lobe of the liver. TheraSphere will be administered through the hepatic artery. The target dose will be 120 Gy + 10%. Dose reduction to a minimum dose of 80 Gy + 10% will be permitted to manage radiation exposure to the lungs. Re-treatment of the same participant/lobe with further cycles of TheraSphere will be permitted if a treatable progression is detected during follow-up evaluations. Any re-treatment will take place at least 28 days after the previous TheraSphere treatment administered to that lobe. Participants can receive a subsequent TheraSphere administration in the absence of radiological progression criteria at the Investigator's discretion. A maximum of 3 TheraSphere administrations will be permitted. |
| Sorafenib | Active comparator | Drug: SorafenibParticipants will receive sorafenib, oral tablets, 400 milligrams (mg) twice daily in accordance with the package insert. Treatment is to continue until the participant is no longer clinically benefiting from therapy or until unacceptable toxicity occurs. Medically appropriate dose adjustments and drug holidays due to adverse events (AEs) and toxicity will be allowed. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (13 listed)
- Participants over 18 years of age, regardless of race or gender
- Advanced unresectable hepatocellular carcinoma with branch portal vein thrombosis (confirmed by non-invasive criteria European Association for the Study of the Liver [EASL]/American Association for the Study of Liver Diseases [AASLD], mandatory by histology in non-cirrhotic participants); can be naive or recurrent HCC after curative treatment ( >6 months before randomization)
- Unilobar disease
- Child Pugh A
- Tumor volume ≤70% of liver volume (determined by visual estimation)
Key exclusion criteria (18 listed)
- Confirmed extra hepatic metastases. Participants with indeterminate hepatic hilar lymph nodes up to 2.5 centimeters (cm) in greatest dimension, or with indeterminate lung nodules (single lesion between 1-1.5 cm, or multiple smaller lesions with a total diameter of ≤2 cm) may be included if metastatic disease is deemed unlikely
- Known contraindication to standard-of-care sorafenib including allergic reaction, pill swallowing difficulty, uncontrolled hypertension or history of cardiac disease, significant GI bleed within 30 days, and renal failure including dialysis
- Evidence of hepatic vein invasion or caval thrombosis
- Evidence of chronic obstructive pulmonary disease
- Indication for any possible curative treatment after multidisciplinary assessment (surgery, ablation, transplantation)
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 |
|---|---|---|
| TheraSphere®Also: yttrium-90 microspheresIntrahepatic treatment of advanced hepatocellular carcinoma | Device | TheraSphere |
| SorafenibAlso: Nexavar®Standard of care therapy for treatment of advanced hepatocellular carcinoma | Drug | Sorafenib |
Primary outcome
Overall Survival (OS) From Time of Randomization
Time frame: Randomization up to participant's death (maximum time = up to Month 30)
OS was calculated as the interval between the randomization date and the date of death for any cause, with censoring at the date of last contact for participants alive.
7 secondary outcomes
Time to Progression (TTP)
Time frame: Randomization up to participant's death (maximum time = up to Month 30)
Time to Worsening Portal Vein Thrombosis (PVT)
Time frame: Baseline (Randomization) up to participant's death (maximum time = up to Month 30)
Time to Symptomatic Progression (TTSP)
Time frame: Randomization up to participant's death (maximum time = up to Month 30)
Number of Participants With Tumor Response
Time frame: Baseline up to participant's death (maximum time = up to Month 30)
Change From Baseline in Quality of Life (QoL) as Assessed by the FACT-Hep Questionnaire
Time frame: Baseline (Randomization), participant's death (maximum time = up to Month 30)
Time to Deterioration QoL (TTDQoL)
Time frame: Baseline (Randomization) up to participant's death (maximum time = up to Month 30)
Number of Participants With Treatment Emergent Adverse Events (TEAE)
Time frame: Randomization up to participant's death (maximum time = up to Month 30)
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 21 Apr 2021.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
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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.
Vincenzo Mazzaferro, MD principal investigator
Istituto Tumori Nazionale, Milan, Italy
Riad Salem, MD principal investigator
Northwestern University
19 sites in 6 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing TheraSphere® and Sorafenib in people with Hepatocellular Carcinoma, run by Boston Scientific Corporation at 19 sites in 6 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 13 inclusion and 18 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: stopped early, as of the sponsor's last update on 21 Apr 2021. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 19 sites in Italy, Spain, United States, United Kingdom, Belgium and 1 more country. 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 29 Oct 2019). 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?
Overall Survival (OS) From Time of Randomization (time frame: Randomization up to participant's death (maximum time = up to Month 30)). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
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 21 Apr 2021.