Clinical Trial Details
— Status: Recruiting
Administrative data
| NCT number |
NCT05808205 |
| Other study ID # |
RP-ALX-01_2019 |
| Secondary ID |
|
| Status |
Recruiting |
| Phase |
|
| First received |
|
| Last updated |
|
| Start date |
June 30, 2021 |
| Est. completion date |
June 30, 2025 |
Study information
| Verified date |
April 2024 |
| Source |
Rose Pharma SA |
| Contact |
n/a |
| Is FDA regulated |
No |
| Health authority |
|
| Study type |
Observational
|
Clinical Trial Summary
This is an open, non-comparative, Single-centre Post Marketing Clinical Followup (PMCF) study
aimed to enrol patients with medium and deep facial sagging, facial volume defects and/or
lips volume and contours defects. The investigation will be useful to collect Investigational
Product' real world safety /performance evidences in normal clinical practice. Each subject,
after signing the Informed Consent, will enter into a 1-week screening phase during which the
baseline tests will be conducted. At baseline visit (Visit 0), as per clinical practice, the
subject can be treated with one or more of the below ALIAXIN products, depending on
investigator clinical evaluation and decision:
- ALIAXIN EV: Essential Volume
- ALIAXIN FL: Lips
- ALIAXIN SR: Shape & Restore
- ALIAXIN GP: Global Performance
- ALIAXIN LV: Lips Volume According the investigator judgment and IP' Instruction For Use
(IFU), each subject can be treated in one or more of following face area:
- Temporal / frontal area
- Orbital / Malar area
- Perioral area
- Lips. For the pre- and post-treatment clinical evaluations, a LifeViz® Mini 3D camera
(QuantifiCare) will be used for face-images capture. A LifeViz® Micro 3D camera
(QuantifiCare) will be used for adjuvant images capture, only in specific conditions
(e.g. nasolabial folds and marionette lines) and according to the Principal Investigator
judgment, to facilitate the clinical evaluation. As per clinical practice, the treatment
can be repeated at touch up visit (Visit 1), after 15 days from Visit 0, according the
investigator clinical evaluation and decision, to maintain/refine the obtained results.
Moreover, after 6 months from Visit 0, as per clinical practice, a visit ( Visit 2, End
of Study Visit) will be performed to collect and evaluate the safety and performance of
treatment(s) performed. Considering the normal clinical practice, after Visit 2,
according the investigator judgment and after a new Informed Consent Form signature, the
subject can be enrolled in a new screening phase as per clinical study design. The
re-enrolled subject should meet all inclusion and none exclusion criteria. In the new
CRF will be reported the previous subject's identification number.
Description:
Aesthetic Dermatology (AD) is a rapidly developing part of dermatology in science and
clinical practice.
The focus, however, needs to be patient-centered and the work scientific to avoid the ethical
dilemma.
The growing patient population and appeal for rapid results have served as an impetus that
transformed the use of soft tissue fillers. While clinicians established innovative ways to
address multidimensional deficiencies of the face, manufacturers developed new formulations
to address the tasks faced by clinicians. With these advancements, it is essential that
facial plastic surgeons are adept at cosmetic applications of soft tissue fillers to provide
quality care and optimize patient outcomes.
Today, there are a variety of injectable soft tissue fillers available for clinical use with
over 160 products belonging to > 50 companies on the market. Factors such as defect type and
location, preferred durationof effect, and clinician expertise with specific agents determine
the most approp riate choice of agent. These fillers can be categorized into resorbable
(biodegradeable), nonresorbable (permanent), and viable autologous fat. Resorbable fillers
include hyaluronic acid (HA), collagen, calcium hydroxylapatite, and poly-L-lactic acid with
HA-based fillers being the most common injectable agents used today. Common permanent fillers
include polymethylmethacrylate (PMMA) microspheres, hydrogel polymers, and silicone
injections. Because most patients are satisfied with temporary filler use, the decision to
pursue permanent fillers must be considered carefully.
Hyaluronic acid (HA) is a naturally occurring polysaccharide frequently used as a functional
ingredient in subcutaneous antiaging treatments, such as dermal fillers, which use the
polymer's unique viscoelastic properties. The major challenge lies in the reasoned choice of
the product to be used depending on the anatomical area to be corrected. Indeed, each region
of the face is subjected to specific mechanical constraints, which the authors take into
account when selecting HA.
Hyaluronic acid can be defined by viscoelasticity and cohesiveness, which will determine the
resistance to deformation during mechanical stresses.
The clinical persistence and characteristics of HA-based dermal fillers may be influenced by
their physical properties. Increasing both the molecular weight and degree of cross-linking
of the polymer is a proven strategy for improving mechanical strength and extending
degradation times.
"ALIAXIN" is a HA-based dermal filler. It is available in five different formulations, with
specific and differentiated visco-elastic properties: ALIAXIN EV (Essential Volume), ALIAXIN
FL (Lips), ALIAXIN SR (Shape & Restore), ALIAXIN GP (Global Performance), ALIAXIN LV (Lips
Volume). Their different behaviours, studied to treat different facial area, are deriving
from the combined use of different molecular weight hyaluronic acids and their crosslinking
degree.
The formulations offered by the "ALIAXIN" line are based on the concept of Hydrolift® Action:
the innovative approach that aims to counteract the reduction of hyaluronic acid in the skin,
restoring hydration, elasticity and skin tone.
"ALIAXIN" has been on the market for many years and in literature are available several
safety and performance clinical data, collected by controlled studies, in which authors
tested "ALIAXIN" or other similar HA-based dermal fillers according the intend of use.
The aim of this open, non-comparative, Single-centre Post Marketing Clinical Follow-up (PMCF)
is to collect "ALIAXIN" real world safety and performance evidences in normal clinical
practice, in the treatment of patients with medium and deep facial sagging, facial volume
defects and/or lips volume and contours defects.
This is a Post-market clinical follow-up Medical Device study
The study objective are the following:
Primary
• To evaluate the re-volumizing performance of the filler ALIAXIN (EV, FL, SR, GP and LV)
used as Intended in patients with facial volume defects.
Secondary
- To evaluate the corrective performance of the filler ALIAXIN (EV, FL, SR, GP and LV)
used as Intended in patients with medium and deep facial sagging;
- To evaluate the safety, tolerability and patient satisfaction of the filler ALIAXIN (EV,
FL, SR, GP and LV).
Methodology: This is an open, non-comparative, Single-centre Post Marketing Clinical
Follow-up (PMCF) study aimed to enrol patients with medium and deep facial sagging, facial
volume defects and/or lips volume and contours defects. The investigation will be useful to
collect Investigational Product' real world safety /performance evidences in normal clinical
practice.
Each subject, after signing the Informed Consent, will enter into a 1-week screening phase
during which the baseline tests will be conducted.
At baseline visit (Visit 0), as per clinical practice, the subject can be treated with one or
more of the below ALIAXIN products, depending on investigator clinical evaluation and
decision:
- ALIAXIN EV: Essential Volume
- ALIAXIN FL: Lips
- ALIAXIN SR: Shape & Restore
- ALIAXIN GP: Global Performance
- ALIAXIN LV: Lips Volume
According the investigator judgment and IP' Instruction For Use (IFU), each subject can be
treated in one or more of following face area:
- Temporal / frontal area
- Orbital / Malar area
- Perioral area
- Lips.
For the pre- and post-treatment clinical evaluations, a LifeViz® Mini 3D camera
(QuantifiCare) will be used for face-images capture.
A LifeViz® Micro 3D camera (QuantifiCare) will be used for adjuvant images capture, only in
specific conditions (e.g. nasolabial folds and marionette lines) and according to the
Principal Investigator judgment, to facilitate the clinical evaluation.
As per clinical practice, the treatment can be repeated at touch up visit (Visit 1), after 15
days from Visit 0, according the investigator clinical evaluation and decision, to
maintain/refine the obtained results.
Moreover, after 6 months from Visit 0, as per clinical practice, a visit ( Visit 2, End of
Study Visit) will be performed to collect and evaluate the safety and performance of
treatment(s) performed.
Considering the normal clinical practice, after Visit 2, according the investigator judgment
and after a new Informed Consent Form signature, the subject can be enrolled in a new
screening phase as per clinical study design. The re-enrolled subject should meet all
inclusion and none exclusion criteria.
In the new CRF will be reported the previous subject's identification number.
Number of subjects (planned and analysed):
Planned: In this study, it is planned to include about 70 patients each year, assuming two
treatments per patient. Due to the post-market nature of the study, this sample size is not
based on a formal statistical sample size calculation, but the size is considered appropriate
for the study purposes and considering the enrollment rate estimated at the center.
To ensure the evaluation of all defined areas, for each 6 months follow-up period, it is
intended that the investigational site will perform a minimum of 5 evaluations for every
identified facial area (i.e., Temporal / frontal area, Orbital / Malar area, Perioral area,
Lips). Considering that each subject can be treated at the same time in one or more facial
area, to reach the 5 evaluations per area, the number of subjects to enrol may vary in every
follow-up period.
Sample size justification: Considering a study duration of 5 years, minimum 200 treatments
will be evaluated. In this study, it is planned to include about 70 patients each year,
assuming two treatments per patient. Due to the post-market/observational nature of the
study, this sample size is not based on a formal statistical sample size calculation, but the
size is considered appropriate for the study purposes and considering the enrollment rate
estimated at the center.
To ensure the evaluation of all defined areas, for each 6 months follow-up period, it is
intended that the investigational site will perform a minimum of 5 evaluations for every
identified facial area (i.e., Temporal / frontal area, Orbital / Malar area, Perioral area,
Lips). Considering that each subject can be treated at the same time in one or more facial
area, to reach the 5 evaluations per area, the number of subjects to enroll may vary in every
follow-up period.
Treatment duration: As per clinical practice, after baseline injection, the treatment can be
repeated only at touch up visit (15 days later) according the investigator clinical
evaluation and decision. After 6 months, at follow-up visit (End of Study), will be performed
the last safety and efficacy evaluation.
Safety Set: this set included all enrolled patients who took at least one does of study
medication.
Full Analysis Set (FAS): this set included all enrolled patients who took at least one dose
of study medication, and with a baseline and at least one post-baseline performance
assessment.
Investigational Product:
- ALIAXIN EV: Essential Volume
- ALIAXIN FL: Lips
- ALIAXIN SR: Shape & Restore
- ALIAXIN GP: Global Performance
- ALIAXIN LV: Lips Volume
They have the same formulation, differentiating only for viscosity in order to better act on
any given district.
Dose/dosage: ALIAXIN fillers are available in a 2ml package with inside 2 sealed blisters,
each containing 1 sterile pre-filled mono-use syringe of 1 ml.
Each IP contain 25mg/ml of Hyaluronic Acid (HA) as their key functional component as
described below:
- ALIAXIN EV, FL, GP and LV: HA cross-linked 25mg/ml
- ALIAXIN SR: HA cross-linked 22.5mg/ml and HA natural 2.5 mg/ml
The volumetric grading printed on the syringe has an indicative value: it is left to the
doctor's discretion to choose the dosage to be used for each individual case.
Administration:
Injection in the medium/deep dermis/ superficial subcutis in accordance to the indication for
use.
The first administration will be performed at baseline. As clinical practice and according
the medical judgment, one or more ALIAXIN filler type (i.e. EV, FL, SR, GP and LV) can be
used for each enrolled subject. Moreover, one or more face area (Temporal / frontal area,
Orbital / Malar area, Perioral area, Lips) can be treated at baseline Visit.
According the normal clinical practices and investigator decision, for the
maintenance/refinement of obtained results it will be possible to repeat the treatment only
at touch up visit (15 days after baseline treatment). The treatment should be repeated
according various factors, regarding both the physiology of the patients (type of skin,
individual metabolism, anatomy, age) and their lifestyle. Another element to consider is
relative to the implant techniques used in the normal clinical practices.
Criteria for evaluation:
Primary efficacy endpoint:
To evaluate the re-volumizing performance of the filler ALIAXIN (EV, FL, SR, GP and LV) used
as Intended in patients with facial volume defects, by treated areas calculating the volume
variation (expressed as cm3) during all study duration compared to baseline volume. A 3D
camera will be used to take subject' face images at all planned visits.
Secondary efficacy endpoints
- To evaluate the corrective performance of the ALIAXIN fillers (EV, FL, SR, GP and LV)
used as Intended in patients with medium and deep facial sagging, performing treated
area evaluation by GAIS scale during all study duration.
- To evaluate the re-volumizing performance of each Filler ALIAXIN (EV, FL, SR, GP and LV)
calculating the volume variation (expressed as cm3) during all study duration compared
to baseline volume. A 3D camera will be used to take subject' face images at all planned
visits.
- To evaluate the tolerability and patient satisfaction of the filler ALIAXIN (EV, FL, SR,
GP and LV) using a 5 Likert Scale during all study duration.
Safety:
Safety will be monitored through vital signs, facial examination and adverse events including
assessment of relationship to the IP.
Time-points for efficacy and safety: Baseline (V0) and all follow up visits performed,
including visits during which administration of the product was repeated.
Interim efficacy and safety analysis: Every year an interim analysis will be completed on
primary and secondary endpoints to periodically evaluate the performance and safety of the
ALIAXIN fillers used as Intended.
Statistical methods: Considering a study duration of 5 years, minimum 200 treatments will be
evaluated.
In general, all the variables will be descriptively analyzed by treated area groups and visit
(mean, median, standard deviation, minimum and maximum for continuous variables after
normality check of distribution with Kolmogorov-Smirnov test, frequency distribution for
categorical variables). All the analysis will be detailed in the Statistical Analysis Plan
(SAP) which will be finalized in Version 1.0 before the Data Base Lock (DBL). Confidence
Intervals (CI) at 95% level will be provided.
In details, the safety data will include (at least) physical examinations, vital signs and
adverse events.
