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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/ct2/show/NCT03148327
Registration number
NCT03148327
Ethics application status
Date submitted
3/05/2017
Date registered
11/05/2017
Date last updated
18/12/2023
Titles & IDs
Public title
Astra Zeneca (Immuno Stereotactic Ablative Body Radiotherapy) ISABR Study: Randomized Phase I/II Study of Stereotactic Body Radiotherapy
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Scientific title
Randomized Phase I/II Study of Ablative Radiotherapy +/- MEDI 4736 (Durvalumab) for Medically Inoperable Early-Stage Non-Small Cell Lung Cancer
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Secondary ID [1]
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NCI-2017-00954
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Secondary ID [2]
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17-000004
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Carcinoma, Non-Small-Cell Lung
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Condition category
Condition code
Cancer
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Lung - Non small cell
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Treatment: Drugs - Durvalumab (MEDI 4736)
Treatment: Other - Radiotherapy
Experimental: Regimen A: Phase I - The intervention will be looking at radiotherapy + drug Durvalumab (MEDI 4736)
Experimental: Regimen A: Phase II - The intervention will be looking at radiotherapy + drug Durvalumab (MEDI 4736)
Active Comparator: Regimen B: Phase II - Radiotherapy alone
Treatment: Drugs: Durvalumab (MEDI 4736)
Early studies has shown to possibly reduce the growth of certain types of lung cancer
Treatment: Other: Radiotherapy
Stereotactic Body Radiation Therapy (SABR)
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Intervention code [1]
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Treatment: Drugs
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Intervention code [2]
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Treatment: Other
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Phase I: The number and severity of study participants' treatment-related adverse events as assessed by CTCAE v4.0.
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Assessment method [1]
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the safety and tolerability associated with radiation therapy and durvalumab (MEDI 4736)
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Timepoint [1]
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4 months
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Primary outcome [2]
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Phase II: Median Progression-Free Survival
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Assessment method [2]
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Progression Free Survival for patients treated with radiation therapy with and without durvalumab (MEDI 4736) will be determined by both the 2-year progression free survival rate (percentage) and the median progression free survival (in years).
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Timepoint [2]
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2 year
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Secondary outcome [1]
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Overall survival
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Assessment method [1]
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the efficacy of radiation therapy and durvalumab in terms of overall survival
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Timepoint [1]
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2 year
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Secondary outcome [2]
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Primary Tumor Control
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Assessment method [2]
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the efficacy of radiation therapy and durvalumab in terms of primary tumor control
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Timepoint [2]
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2 year
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Secondary outcome [3]
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Intralobar recurrence rates
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Assessment method [3]
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the efficacy of radiation therapy and durvalumab in terms of intralobar recurrence rates
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Timepoint [3]
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2 year
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Secondary outcome [4]
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mediastinal recurrences
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Assessment method [4]
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the efficacy of radiation therapy and durvalumab in terms of mediastinal recurrences
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Timepoint [4]
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2 year
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Secondary outcome [5]
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hilar and mediastinal recurrences
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Assessment method [5]
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the efficacy of radiation therapy and durvalumab in terms of hilar and mediastinal recurrences
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Timepoint [5]
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2 year
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Secondary outcome [6]
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rate of distant recurrences
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Assessment method [6]
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the efficacy of radiation therapy and durvalumab (MEDI 4736) in terms of the rate of distant recurrences
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Timepoint [6]
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2 years
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Secondary outcome [7]
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rates of grade 3 or higher non-hematological toxicities
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Assessment method [7]
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rates of grade 3 or higher non-hematological toxicities with the combination of radiation therapy and durvalumab MEDI 4736)
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Timepoint [7]
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2 years
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Eligibility
Key inclusion criteria
For inclusion in the study subjects must fulfill all of the following criteria:
1. Written informed consent obtained from the patient/legal representative prior to
performing any protocol-related procedures, including screening evaluation.
2. Newly diagnosed, untreated, biopsy proven non-small cell lung cancer.
3. Medically inoperable or patient refusal to surgery as defined by any single of the
following criteria: a. Determined unfit for surgery by thoracic surgeon or radiation
oncologist as documented in the medical record b. Pulmonary function test (PFTS)
showing Forced Expiratory Volume in the first second (FEV1) = 1.2 L or diffusing Lung
Capacity (DLC) <60%, c. Poor exercise tolerance or failed pre-operative cardiac
work-up, d. Patient refusal to undergo definitive surgery as documented in clinical
note by a surgeon, pulmonologist, medical oncologist, or radiation oncologist.
4. Clinically stage I disease by American Joint Committee on Cancer (AJCC) 7th edition.
(N0, M0, T stages T1-T2a) or patients with stage T2bN0M0 (clinical stage IIA) disease
who are medically unfit for standard of care chemotherapy as documented by a medical
oncologist or radiation oncologist, or who refuse standard of care chemotherapy as
documented by a medical oncologist or radiation oncologist.
5. Age > 18 years at time of study entry.
6. Eastern Cooperative Oncology Group (ECOG) performance status of 0 - 1.
7. Adequate normal organ and marrow function as defined below:
- Haemoglobin = 9.0 g/dL.
- Absolute neutrophil count (ANC) = 1.5 x 109/L (> 1500 per mm3).
- Platelet count = 100 x 109/L (>100,000 per mm3).
- Serum bilirubin = 1.5 x institutional upper limit of normal (ULN). <<This will
not apply to subjects with confirmed Gilbert's syndrome (persistent or recurrent
hyperbilirubinemia that is predominantly unconjugated in the absence of hemolysis
or hepatic pathology), who will be allowed only in consultation with their
physician.>>
- aspartate aminotransferase (AST) serum glutamic oxaloacetic transaminase (SGOT)/
alanine aminotransferase (ALT) serum glutamic pyruvic transaminase (SGPT) = 2.5 x
institutional upper limit of normal unless liver metastases are present, in which
case it must be = 5x ULN.
- Serum creatinine creatinine clearance (CL) >40 mL/min by the Cockcroft-Gault
formula (Cockcroft and
Gault 1976) or by 24-hour urine collection for determination of creatinine clearance:
Males:
Creatinine CL (mL/min)
= Weight (kg) x (140 - Age) . 72 x serum creatinine (mg/dL)
Females:
Creatinine CL (mL/min)
= Weight (kg) x (140 - Age) x 0.85 72 x serum creatinine (mg/dL)
8. Female subjects must either be of non-reproductive potential (i.e. post-menopausal by
history: =60 years old and no menses for =1 year without an alternative medical cause;
OR history of hysterectomy, OR history of bilateral tubal ligation, OR history of
bilateral oophorectomy) or must have a negative serum pregnancy test upon study entry.
9. Subject is willing and able to comply with the protocol for the duration of the study
including undergoing treatment and scheduled visits and examinations including follow
up.
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
1. ECOG Performance status >1.
2. Patients with metastatic or node positive NSCLC.
3. Patients with prior radiation therapy to the same bronchopulmonary segment.
4. History of automimmune disease including myasthenia gravis, myositis, autoimmune
hepatitis, systemic lupus erythematous, rheumatoid arthritis, inflammatory bowel
disease (e.g., Crohn's disease, ulcerative colitis), vascular thrombosis associated
with antiphospholipid syndrome, Wegner's granulomatosis, Sjogren's syndrome,
Guillain-Barre syndrome, multiple sclerosis, or glomerulonephritis.
a. However, patients with type 1 diabetes mellitus, vitiligo, alopecia, hypothyroidism
requiring hormone replacement, Graves disease, or skin disorders not requiring
systemic treatment are permitted to enroll.
5. Patients with history of idiopathic pulmonary fibrosis, idiopathic pneumonitis, drug
induced pneumonitis, or evidence of active pneumonitis on screening chest CT scan.
6. Involvement in the planning and/or conduct of the study (applies to both AstraZeneca
staff and/or staff at the study site).
7. Participation in another clinical study with an investigational product during the
last 6 months.
8. Any previous treatment with a Programmed Death-1 (PD1) or Programmed Death-Ligand
1(PD-L1) inhibitor, including durvalumab, and therapeutic anticancer vaccine.
9. History of another primary malignancy except for:
1. Malignancy treated with curative intent and with no known active disease =5 years
before the first dose of study drug and of low potential risk for recurrence.
2. Adequately treated non-melanoma skin cancer or lentigo maligna without evidence
of disease.
3. Adequately treated carcinoma in situ without evidence of disease e.g., cervical
cancer in situ.
10. Mean QT interval corrected for heart rate (QTc) =470 ms calculated from 3
electrocardiograms (ECGs) using Frediricia's Correction.
11. Current or prior use of immunosuppressive medication within 28 days before the first
dose of durvalumab, with the exceptions of intranasal and inhaled corticosteroids or
systemic corticosteroids at physiological doses, which are not to exceed 10 mg/day of
prednisone, or an equivalent corticosteroid.
12. Any unresolved = Grade 2 pulmonary toxicity from previous anti-cancer therapy.
13. Any prior Grade =3 immune-related adverse event (irAE) while receiving any previous
immunotherapy agent, or any unresolved irAE >Grade 1.
14. History of primary immunodeficiency.
15. History of allogeneic organ transplant.
16. History of hypersensitivity to durvalumab or any excipient.
17. Uncontrolled intercurrent illness including, but not limited to, ongoing or active
infection, symptomatic congestive heart failure, uncontrolled hypertension, unstable
angina pectoris, cardiac arrhythmia, active peptic ulcer disease or gastritis, active
bleeding diatheses including any subject known to have evidence of acute or chronic
hepatitis B, hepatitis C or human immunodeficiency virus (HIV), or psychiatric
illness/social situations that would limit compliance with study requirements or
compromise the ability of the subject to give written informed consent.
18. Known history of previous clinical diagnosis of tuberculosis.
19. History of leptomeningeal carcinomatosis.
20. Receipt of live attenuated vaccination within 30 days prior to study entry or within
30 days of receiving durvalumab.
21. Female subjects who are pregnant, breast-feeding or male or female patients of
reproductive potential who are not employing an effective method of birth control.
22. Any condition that, in the opinion of the investigator, would interfere with
evaluation of study treatment or interpretation of patient safety or study results.
23. Subjects with uncontrolled seizures. -
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
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Phase
Phase 1/Phase 2
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Active, not recruiting
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
11/10/2017
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
1/06/2025
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Actual
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Sample size
Target
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Accrual to date
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Final
18
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Recruitment in Australia
Recruitment state(s)
VIC
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Recruitment hospital [1]
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Peter MacCallum Cancer Centre - Melbourne E.
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Recruitment postcode(s) [1]
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3000 - Melbourne E.
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Recruitment outside Australia
Country [1]
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United States of America
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State/province [1]
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California
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Country [2]
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United States of America
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State/province [2]
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Colorado
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Country [3]
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United States of America
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State/province [3]
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New York
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Funding & Sponsors
Primary sponsor type
Other
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Name
Jonsson Comprehensive Cancer Center
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Address
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Country
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Other collaborator category [1]
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Commercial sector/Industry
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Name [1]
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AstraZeneca
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Address [1]
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Country [1]
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Ethics approval
Ethics application status
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Summary
Brief summary
This study uses durvalumab (MEDI 4736), an experimental type of drug made by Astra Zeneca
Pharmaceuticals, (limited partnership) LP, which in early studies has shown to possibly
reduce the growth of certain types of lung cancer. The Investigators will enroll up to 105
subjects into the study. After an initial safety sample of 15 individuals receiving
durvalumab (MEDI 4736) and Stereotactic Ablative Body Radiotherapy (SABR), if it is shown to
be safe to administer this combination of therapies, the next enrolled subjects will be
randomized in a 1:1 fashion (each subject with a "50-50 chance" like the flip of a coin) to
receive either SABR and durvalumab (MEDI 4736), or SABR alone.
Once treatment is completed, all subjects will return to the University of California at Los
Angeles (UCLA) for regular follow-up visits to check on their health and outcomes. At visits
both prior to and after treatment special blood samples will be drawn to be studied by UCLA
scientists to look into the basic science aspects of how durvalumab (MEDI 4736) and radiation
work in the body. It is hoped that we will learn more about the basic safety and science of
durvalumab (MEDI 4736) combined with Stereotactic Ablative Body Radiotherapy (SABR) vs. SABR
alone, while extending the life and quality of life of these subjects.
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Trial website
https://clinicaltrials.gov/ct2/show/NCT03148327
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
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Ann Raldow, MD
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Address
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Associate Professor
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Fax
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Email
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Contact person for public queries
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Fax
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Contact person for scientific queries
Summary Results
For IPD and results data, please see
https://clinicaltrials.gov/ct2/show/NCT03148327
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