OCTOPUS: A Study to Assess the Effects of Brolucizumab in Adult Patients With Neovascular Age Related Macular Degeneration
Study Details
Study Description
Brief Summary
Neovascular age-related macular degeneration (nAMD) is characterized by the presence of choroidal neovascularization (CNV). Choroidal neovascularization consists of abnormal blood vessels originating from the choroid and can lead to hemorrhage, fluid exudation, and fibrosis, resulting in photoreceptor damage and vision loss.
The safety and efficacy of brolucizumab has been demonstrated in 2 randomized, multicenter, double-masked, active controlled Phase 3 studies in nAMD patients (RTH258-C001 and RTH258-C002). Anatomical changes were evaluated in these studies using spectral domain optical coherence tomography (SD-OCT), which relied on indirect parameters for the diagnosis of active CNV. The OCT-angiography (OCT A) that directly visualize retinal circulation and image CNV and vascular diseases of the retina was not included in previous brolcuizumab studies.
This single-arm, open-label, multicenter study is being performed to evaluate the efficacy and safety of brolucizumab 6 mg in patients with nAMD.
OCT-A will be used in this study to assess the morphological response of patients to brolucizumab in terms of percentage change in CNV lesion area in the short term (i.e. at Week 12) and in the long term (i.e. at Week 48), as well as changes in other OCT-A features up to Week 48.
Approximately 210 adult patients will be screened and included in centers in France.
The maximum study duration for 1 patient is 48 weeks.
Patients will be required to attend 6 mandatory study visits: Screening/Baseline Visit (Day 1), Week 4, Week 8, Week 12, Week 16 and Week 48 visits. The timing of the interim visits between Week 16 and Week 48 will depend on the patient's injection regimen, i.e. every 8 weeks or every 12 weeks according to disease activity assessed by the investigator.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
| Phase 3 |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: RTH258/Brolucizumab This is a single-arm study in which all patients will be treated with brolucizumab 6mg: 3 loading injections (at Screening/Baseline, Week 4 and Week 8), followed by maintenance treatment from Week 16/Week 20 up to Week 40/Week 44. |
Drug: RTH258/Brolucizumab
Brolucizumab is a new generation of anti-VEGF (vascular endothelial growth factor). All patients will be treated with brolucizumab 6mg: 3 loading injections (at Screening/Baseline, Week 4 and Week 8), followed by maintenance treatment from Week 16/Week 20 up to Week 40/Week 44.
|
Outcome Measures
Primary Outcome Measures
- Percentage change in CNV lesion area measured by OCT-A from Baseline to Week 12 [Week 12]
To evaluate the short-term effect of brolucizumab on CNV lesion area as measured by Optical Coherence Tomography Angiography (OCT-A) in nAMD patients.
Secondary Outcome Measures
- Percentage change in CNV lesion area measured by OCT-A from Baseline to Week 48 [Week 48]
To evaluate the long-term effects of brolucizumab on Choroidal Neovascularization (CNV) morphology as measured by OCT-A in nAMD patients.
- Change in OCT-A features assessed by qualitative and quantitative criteria from Baseline by visit at Week 12 up to Week 48 [Week 48]
To evaluate the long-term effects of brolucizumab on Choroidal Neovascularization (CNV) morphology as measured by OCT-A in nAMD patients.
- Change in SD-OCT and FA features assessed by qualitative and quantitative criteria: Central Sub-Field Retinal Thickness (CSFT), sub and/or intraretinal fluid, sub-RPE (Retinal Pigmented Epithelium) fluid from Baseline by visit up to Week 48 [Week 48]
To evaluate the effect of brolucizumab on anatomical parameters as assessed by Spectral Domain Optical Coherence Tomography (SD-OCT) and Fluorescein Angiography (FA) from Week 12 up to Week 48.
- Change in Best Corrected Visual Acuity (BCVA) from Baseline up to Week 48 [Week 48]
To evaluate the efficacy of brolucizumab up to Week 48 by assessing changes in BCVA.
- Proportion of patients who are maintained on an exclusive treatment interval every 12 weeks (q12w) following the loading phase through to Week 48 [Week 48]
To estimate the proportion of patients treated at q12w frequency with brolucizumab.
- The probability of the first q12w interval for determining successful q12w maintenance at Week 48 [Week 48]
To estimate the predictive value of the first q12w cycle for maintenance of q12w treatment with brolucizumab.
- Time from last Intravitreal (IVT) injection in the initiation phase to first visit with no disease activity. [Week 8 until Week 48]
To evaluate the time from last IVT injection in the initiation phase to first visit with no disease activity.
Eligibility Criteria
Criteria
INCLUSION Criteria:
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Patients must provide written informed consent before any study related procedures are performed.
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Patients must be 50 years of age or older at Screening/Baseline.
Study eye:
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Active CNV lesions secondary to AMD that affect the central subfield, including retinal angiomatous proliferation (RAP) with a CNV component, confirmed by presence of active leakage from CNV seen by fluorescein angiography and sequellae of CNV, e.g. pigment epithelial detachment (PED), subretinal hemorrhage or sub-retinal pigment epithelium (sub-RPE) hemorrhage, blocked fluorescence, macular edema.
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Intra- and/or subretinal fluid affecting the central subfield of the study eye at Screening/Baseline.
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BCVA between 83 and 23 letters, inclusive, in the study eye at Screening/Baseline using early treatment diabetic retinopathy study (ETDRS) at an initial testing distance of 4 meters.
EXCLUSION Criteria:
Ocular conditions:
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Any active intraocular or periocular infection or active intraocular inflammation (e.g. infectious conjunctivitis, keratitis, scleritis, endophthalmitis, infectious blepharitis) in either eye at Screening/Baseline.
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Presence of amblyopia, amaurosis or ocular disorders in the fellow eye with BCVA < 35 ETDRS letters at Screening (except when due to conditions whose surgery may improve visual acuity, e.g. cataract).
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Medical history of intraocular inflammation and/or retinal vascular occlusion within 12 months prior to Screening/Baseline.
Study eye:
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Poor quality of OCT-A and SD-OCT images at Screening/Baseline.
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Atrophy or fibrosis involving the center of the fovea in the study eye, as assessed by color fundus photography and fundus autofluorescence (FAF) at Screening/Baseline.
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The total area of fibrosis or subretinal blood affecting the foveal center point comprising ≥ 50% of the lesion area in the study eye at Screening/Baseline.
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Concomitant conditions or ocular disorders in the study eye, including retinal diseases other than nAMD, that, in the judgment of the investigator, could require medical or surgical intervention during the course of the study to prevent or treat visual loss that might result from that condition, or that limits the potential to gain visual acuity upon treatment with the investigational product.
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Structural damage within 0.5 disc diameter of the center of the macula in the study eye, e.g. vitreomacular traction, epiretinal membrane, retinal pigment epithelium (RPE) rip/tear scar, laser burn, at the time of Screening that in the investigator's opinion could preclude visual function improvement with treatment.
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Current vitreous hemorrhage or history of vitreous hemorrhage in the study eye within 4 weeks prior to Screening/Baseline.
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Uncontrolled glaucoma in the study eye defined as IOP > 25 mmHg on medication or according to the investigator's judgment at Screening/Baseline.
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Aphakia and/or absence of the posterior capsule in the study eye at Screening/Baseline.
Ocular treatments (study eye):
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Patient has received any approved or investigational treatment for nAMD (other than vitamin supplements) in the study eye at any time.
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Intraocular or periocular use of corticosteroids in the study eye during the 6-month period prior to Screening/Baseline.
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Previous penetrating keratoplasty or vitrectomy at any time prior to Screening/Baseline.
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History or evidence of the following in the study eye within the 90-day period prior to Screening/Baseline:
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Intraocular or refractive surgery.
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Previous panretinal photocoagulation.
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Previous submacular surgery, other surgical intervention or laser treatment for nAMD including photodynamic therapy (PDT).
Systemic conditions or treatments:
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End stage renal disease requiring dialysis or renal transplant.
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Systemic medications known to be toxic to the lens, retina or optic nerve (e.g. deferoxamine, chloroquine/hydroxychloroquine, tamoxifen, phenothiazines and ethambutol) used during the 6-month period prior to Screening/Baseline except temporary use for COVID-19 treatment.
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Participation in an investigational drug, biologic, or device study within 30 days or the duration of 5 half-lives of the investigational product (whichever is longer) prior to Screening/Baseline. Note: observational clinical studies solely involving over-the-counter vitamins, supplements, or diets are not exclusionary.
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Systemic anti-VEGF therapy at any time.
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Stroke or myocardial infarction in the 6-month period prior to Screening/Baseline.
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Uncontrolled blood pressure defined as a systolic value ≥ 160 mmHg or diastolic value ≥ 100 mmHg at Screening/Baseline. (In case there is an elevated blood pressure measurement, it should be repeated after 20 minutes. If the repeat measurement is elevated, then the patient is not eligible to be enrolled into the study).
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History of a medical condition (disease, metabolic dysfunction with exception of type 1 or 2 diabetes mellitus, physical examination finding, or clinical laboratory finding) that, in the judgment of the investigator, would preclude scheduled study visits, completion of the study, or a safe administration of investigational product.
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History of malignancy of any organ system (other than localized basal cell carcinoma of the skin or in situ cervical cancer), treated or untreated, within the past 5 years, regardless of whether there is evidence of local recurrence or metastases.
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History of hypersensitivity to any component of the test article, control article, or clinically relevant sensitivity to fluorescein dye, as assessed by the investigator.
Other:
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Pregnant or nursing (lactating) women, where pregnancy is defined as the state of a female after conception and until the termination of gestation, confirmed by a positive human chorionic gonadotropin (hCG) pregnancy test.
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Women of childbearing potential, defined as all women less than 1 year postmenopausal or less than 6 weeks since sterilization at Screening/Baseline Women are considered post-menopausal and not of childbearing potential if they have had 12 months of natural (spontaneous) amenorrhea with an appropriate clinical profile (e.g. age appropriate history of vasomotor symptoms) or have had surgical bilateral oophorectomy (with or without hysterectomy), total hysterectomy, or tubal ligation at least 6 weeks before taking study treatment. In the case of oophorectomy alone, only when the reproductive status of the woman has been confirmed by follow-up hormone level assessment is she considered not of childbearing potential.
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Patients mentioned in Articles L.1121-5 to L.1121-8 and L.1122-1-2 of the Code de Santé Publique (e.g. minors, protected adults, etc.)
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Novartis Investigative Site | Nice | Cedex1 | France | 06001 |
| 2 | Novartis Investigative Site | Rennes Cedex 9 | FRA | France | 35033 |
| 3 | Novartis Investigative Site | Saint Cyr sur Loire | Indre Et Loire | France | 37540 |
| 4 | Novartis Investigative Site | Bobigny cedex | Seine Saint Denis | France | 93009 |
| 5 | Novartis Investigative Site | Aix en Provence | France | 13090 | |
| 6 | Novartis Investigative Site | Angers | France | 49044 | |
| 7 | Novartis Investigative Site | Avignon | France | 84000 | |
| 8 | Novartis Investigative Site | Bordeaux | France | 33000 | |
| 9 | Novartis Investigative Site | Boulogne-sur-Mer | France | 62321 | |
| 10 | Novartis Investigative Site | Caen Cedex | France | 14033 | |
| 11 | Novartis Investigative Site | Caen | France | 14000 | |
| 12 | Novartis Investigative Site | Creteil | France | 94000 | |
| 13 | Novartis Investigative Site | Dijon | France | 21034 | |
| 14 | Novartis Investigative Site | Floirac | France | 33270 | |
| 15 | Novartis Investigative Site | Grenoble | France | 38000 | |
| 16 | Novartis Investigative Site | La Rochelle | France | 17019 | |
| 17 | Novartis Investigative Site | Lagord | France | 17140 | |
| 18 | Novartis Investigative Site | Le Chesnay | France | 78157 | |
| 19 | Novartis Investigative Site | Lille | France | 59000 | |
| 20 | Novartis Investigative Site | Lyon Cedex 04 | France | 69317 | |
| 21 | Novartis Investigative Site | Lyon | France | 69002 | |
| 22 | Novartis Investigative Site | Marseille | France | F 13008 | |
| 23 | Novartis Investigative Site | Montargis | France | 45200 | |
| 24 | Novartis Investigative Site | Montauban | France | 82000 | |
| 25 | Novartis Investigative Site | Montpellier | France | 34000 | |
| 26 | Novartis Investigative Site | Mulhouse cedex | France | 68070 | |
| 27 | Novartis Investigative Site | Nantes Cedex 1 | France | 44093 | |
| 28 | Novartis Investigative Site | Nantes | France | 44300 | |
| 29 | Novartis Investigative Site | Paris cedex 10 | France | 75010 | |
| 30 | Novartis Investigative Site | Paris | France | 75007 | |
| 31 | Novartis Investigative Site | Perpignan | France | 66000 | |
| 32 | Novartis Investigative Site | Plerin | France | 22190 | |
| 33 | Novartis Investigative Site | Poitiers | France | 86021 | |
| 34 | Novartis Investigative Site | Rouen | France | 76100 | |
| 35 | Novartis Investigative Site | Royan | France | 17200 | |
| 36 | Novartis Investigative Site | Rueil Malmaison | France | 92500 | |
| 37 | Novartis Investigative Site | Saint Herblain | France | 44819 | |
| 38 | Novartis Investigative Site | Saint Martin des Champs | France | 50300 | |
| 39 | Novartis Investigative Site | Strasbourg | France | 67000 | |
| 40 | Novartis Investigative Site | Toulouse Cedex 9 | France | 31059 |
Sponsors and Collaborators
- Novartis Pharmaceuticals
Investigators
- Study Director: Novartis Pharmaceuticals, Novartis Pharmaceuticals
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- CRTH258AFR01
- 2019-003338-17