Melanoma Stage IVBERINGNCT04045691
Binimetinib Plus Encorafenib Real Life Investigation of Next Generation Melanoma Treatment
An observational study of Melanoma Stage IV and Melanoma Stage III, run by Pierre Fabre Pharma GmbH at 59 sites in 3 countries.
Trial summary
BERING-MELANOMA - designed as a prospective, longitudinal, non-interventional study - investigates real-world effectiveness, quality of life, safety and tolerability of encorafenib plus binimetinib in unresectable advanced or metastatic BRAF(Rapidly Accelerated Fibrosarcoma isoform B)-V600-mutant malignant melanoma… Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Melanoma Stage IV, Melanoma Stage III
- What is being tested?
- Encorafenib and Binimetinib
- How many people
- 750 participants
- Where
- 59 sitesin 3 countries
- Study dates
- 17 Oct 2019to Sep 2027
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
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
Study population: Adult patients with unresectable advanced or metastatic BRAFV600-mutant malignant melanoma, with a decision to receive targeted treatment with Encorafenib/Binimetinib according to the current SmPC.
Who may be able to join
- Written informed consent of the patient with regard to the pseudonymized documentation as well as the transfer and processing of his/her data within the study and the ADOREG [Cancer Registry of German Working Group of Dermato-Oncology] registry (data transfer to ADOREG registry only for patients from German sites);
- Legally capable male or female patient ≥ 18 years of age (no upper limit);
- Decision was taken to treat the patient with encorafenib plus binimetinib in accordance with the current SmPC [Summary of Product Characteristics] and by prescription; this decision was taken prior to and independent from the inclusion into the study;
- Treatment with encorafenib plus binimetinib has been started ≤ 6 months prior to providing written informed consent for this study or is planned to be started in the near future;
- Unresectable advanced or metastatic malignant melanoma with BRAF [Rapidly Accelerated Fibrosarcoma isoform B] V600 mutation;
- Treatment-naive or after one prior line of checkpoint inhibitor treatment (anti-CTLA4 [Cytotoxic T-Lymphocyte Antigen-4] and/or anti-PD(L)1 [Programmed cell Death protein 1]) in the unresectable advanced or metastatic setting.
Who cannot join
- Previous treatment with a BRAF- and/or MEK [Mitogen-Activated Protein/Extracellular-signal Regulated Kinase]- inhibitor except for:
- -- prior adjuvant treatment with BRAF+MEK-inhibitor combination therapy that ended > 6 months prior start of Encorafenib/Binimetinib treatment;
- More than one prior line of checkpoint inhibitor treatment in the unresectable advanced or metastatic setting;
- Any previous chemotherapeutic treatment of the melanoma disease;
- Presence of any contraindication with regard to the encorafenib-binimetinib-treatment as specified in the corresponding SmPCs;
- Current or upcoming participation in an interventional clinical trial;
- Current or upcoming systemic treatment of any other tumor than melanoma;
- Prisoners or persons who are compulsorily detained (involuntarily incarcerated).
Trial locations and contacts
59 sites in 3 countries. Contact the study team or a site near you to ask about taking part.
59 sites in 3 countries
Germany42 sites, 42 recruiting
- Recruiting
45
Ahaus
- Recruiting
8
Aschaffenburg
- Recruiting
56
Augsburg
- Recruiting
51
Berlin
- Recruiting
27
Bremerhaven
- Recruiting
1
Buxtehude
- Recruiting
43
Chemnitz
- Recruiting
34
Donauwörth
- Recruiting
49
Dresden
- Recruiting
47
Duisburg
- Recruiting
40
Erfurt
- Recruiting
20
Essen
- Recruiting
9
Gera
- Recruiting
28
Giessen
- Recruiting
42
Goslar
- Recruiting
59
Göttingen
- Recruiting
19
Hamburg
- Recruiting
21
Hanover
- Recruiting
2
Heidelberg
- Recruiting
33
Karlsruhe
- Recruiting
39
Kiel
- Recruiting
29
Landshut
- Recruiting
44
Leipzig
- Recruiting
4
Lübeck
- Recruiting
30
Ludwigshafen
- Recruiting
46
Magdeburg
- Recruiting
15
Mainz
- Recruiting
5
Mannheim
- Recruiting
57
Marburg
- Recruiting
6
Minden
- Recruiting
31
München
- Recruiting
7
München
- Recruiting
16
Münster
- Recruiting
35
Münster
- Recruiting
18
Nuremberg
- Recruiting
50
Regensburg
- Recruiting
41
Schorndorf
- Recruiting
17
Schwerin
- Recruiting
48
Stolberg
- Recruiting
55
Trier
- Recruiting
54
Tübingen
- Recruiting
32
Zwickau
Austria9 sites, 9 recruiting
- Recruiting
11
Graz
- Recruiting
13
Innsbruck
- Recruiting
14
Klagenfurt
- Recruiting
10
Linz
- Recruiting
3
Linz
- Recruiting
12
Salzburg
- Recruiting
22
Vienna
- Recruiting
53
Vienna
- Recruiting
23
Wiener Neustadt
Switzerland8 sites, 8 recruiting
- Recruiting
38
Aarau
- Recruiting
52
Bellinzona, Canton Ticino, 6500
- Recruiting
37
Bern, 3010
- Recruiting
24
Chur
- Recruiting
36
Lausanne
- Recruiting
58
Lucerne, 6000
- Recruiting
26
Winterthur
- Recruiting
25
Zurich
About this study
Official title: Encorafenib Plus Binimetinib in Patients With Locally Advanced, Unresectable or Metastatic BRAFV600-mutated Melanoma: a Multi-centric, Multinational, Prospective, Longitudinal, Non-interventional Study in Germany, Austria and Switzerland - BERING MELANOMA
BERING-MELANOMA - designed as a prospective, longitudinal, non-interventional study - investigates real-world effectiveness, quality of life, safety and tolerability of encorafenib plus binimetinib in unresectable advanced or metastatic BRAF(Rapidly Accelerated Fibrosarcoma isoform B)-V600-mutant malignant melanoma after commercial availability of these two products in Germany, Austria and Switzerland. The study focusses on the documentation of the first and second line setting (i.e. after one line of prior checkpoint inhibition) by documenting patients treated according to the SmPC (Summary of Product Characteristics).
- Conditions
- Melanoma Stage IV, Melanoma Stage III
- Being tested
- Encorafenib, Binimetinib
- Keywords
- BERING, Encorafenib, Binimetinib
- Medical subject headings
- Melanoma
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
EncorafenibDrug
Observation of real-life treatment with encorafenib and binimetinib
BinimetinibDrug
Observation of real-life treatment with encorafenib and binimetinib
What is being measured
The primary outcome is the main question the study is designed to answer.
Progression-free survival
Progression-free survival rate
Measured: At 12 months after start of treatment
Secondary outcomes (24)
Patient and disease profiles at start of treatment with encorafenib plus binimetinib
Demographic and disease characteristics
Measured: Baseline
Type of treatments before and after encorafenib plus binimetinib
Treatment sequence prior to and after encorafenib plus binimetinib; by documenting pre-treatments with adjuvant therapy and systemic therapy in palliative setting; and by documenting subsequent systemic treatment lines after administration of encorafenib plus binimetinib
Measured: Complete observation time-frame (the total observation period of this study will amount to 90 months).
Sequence of treatments before and after encorafenib plus binimetinib
Treatment sequence prior to and after encorafenib plus binimetinib; by documenting pre-treatments with adjuvant therapy and systemic therapy in palliative setting; and by documenting subsequent systemic treatment lines after administration of encorafenib plus binimetinib
Measured: Complete observation time-frame (the total observation period of this study will amount to 90 months).
Characteristics of treatment with encorafenib plus binimetinib
Evaluation of reason for treatment selection (efficacy, safety profile, quality of life, patients preference, physician's preference, comorbidities, other)
Measured: From start to end of treatment (anticipated median treatment duration ca. 12 months)
Effectiveness of treatment with encorafenib plus binimetinib
Further progression-free survival parameters
Measured: From start to end of treatment (anticipated median treatment duration ca. 12 months)
Effectiveness of treatment with encorafenib plus binimetinib
Time-to-progression
Measured: From start to end of treatment (anticipated median treatment duration ca. 12 months)
Effectiveness of treatment with encorafenib plus binimetinib
Best observed tumor response
Measured: From start to end of treatment (anticipated median treatment duration ca. 12 months)
Effectiveness of treatment with encorafenib plus binimetinib
Overall response rate
Measured: From start to end of treatment (anticipated median treatment duration ca. 12 months)
Effectiveness of treatment with encorafenib plus binimetinib
Duration of response
Measured: From start to end of treatment (anticipated median treatment duration ca. 12 months)
Effectiveness of treatment with encorafenib plus binimetinib
Disease control rate
Measured: From start to end of treatment (anticipated median treatment duration ca. 12 months)
Effectiveness of treatment with encorafenib plus binimetinib
Duration of disease control
Measured: From start to end of treatment (anticipated median treatment duration ca. 12 months)
Effectiveness of treatment with encorafenib plus binimetinib
Overall survival
Measured: Complete observation time-frame (the total observation period of this study will amount to 90 months).
Patient reported outcomes during treatment with encorafenib plus binimetinib - evaluated with EORTC QLQ C-30
EORTC QLQ C-30 questionnaires (European Organisation for Research and Treatment of Cancer Quality of Life C-30 questionnaires) to assess quality of life of cancer patients; comprises 30 items, 24 of which are aggregated into nine multi-item scales, that is, five functioning scales (physical, role, cognitive, emotional and social), three symptom scales (fatigue, pain and nausea/vomiting) and one global health status scale. The remaining six single-item (dyspnoea, appetite loss, sleep disturbance, constipation, diarrhoea and the financial impact) scales assess symptoms.
Measured: From start to end of treatment (anticipated median treatment duration ca. 12 months)
Patient reported outcomes during treatment with encorafenib plus binimetinib evaluated with WPAI
WPAI questionnaires (Work Productivity and Activity Impairment questionnaires). The following questions ask about the effect of patients melanoma on the ability to work and perform regular activities.
- Are you currently employed (working for pay)?
- During the past seven days, how many hours did you miss from work because of problems associated with your melanoma?
- During the past seven days, how many hours did you miss from work because of any other reason?
- During the past seven days, how many hours did you actually work?
- During the past seven days, how much did your melanoma affect your productivity while you were working?
- During the past seven days, how much did your melanoma affect your ability to do your regular daily activities, other than work at a job?
Measured: From start to end of treatment (anticipated median treatment duration ca. 12 months)
Patient reported outcomes during treatment with encorafenib plus binimetinib evaluated with CTSQ
CTSQ questionnaires (Cancer Therapy Satisfaction Questionnaire) to assess patients' opinions and feelings concerning their cancer therapy and associated adverse events:
- Questions to patients thoughts about cancer therapy (IV/pills). Scale: [Always, Most of the time, Some-times, Rarely, Never];
- Questions to patients satisfaction with the most recent cancer therapy (IV/pills):
- Scale reg. benefit: [Much better than my expectations Somewhat better than my expectations, Met my expectations, Somewhat worse than my expectations, Much worse than my expectations];
- Scale reg. side effects: [Much better than I expected, Somewhat better than I expected, Exactly as I expected, Somewhat worse than I expected, Much worse than I expected];
- Scale reg. satisfaction: [Very satisfied, Satisfied, Neither satisfied nor dissatisfied, Dissatisfied, Very dissatisfied];
- Scale reg. choice of therapy: [Yes, definitely, Probably Yes, I don't know, Probably not, Definitely not]
Measured: From start to end of treatment (anticipated median treatment duration ca. 12 months)
Physicians' satisfaction with regard the treatment with encorafenib plus binimetinib
Physicians' satisfaction questionnaires (measuring Physician's Satisfaction with regard to Effictiveness and Safety, as well as Physician's Overall Treatment Satisfaction) using the following scale construct:
- Physician's Satisfaction with regard to Efficiency
- Physician's Satisfaction with regard to Safety
- Physician's Overall Treatment Satisfaction
Scale:
- very dissatisfied
- dissatisfied
- moderately satisfied
- satisfied
- very satisfied
Measured: From start to end of treatment (anticipated median treatment duration ca. 12 months)
Safety and tolerability of treatment with encorafenib plus binimetinib - Adverse events and adverse reactions including time to onset and time to resolution
Number of patients with Adverse Events and maximum grade per patient, Adverse Drug Reactions, Adverse Drug Reactions grade 3/4, Serious Adverse Events, Serious Adverse Drug Reactions.
Measured: Complete observation time-frame (the total observation period of this study will amount to 90 months).
Prognostic factors
Influence of prognostic factors on quality of life outcome parameters
Measured: Complete observation time-frame (the total observation period of this study will amount to 90 months).
Prognostic factors
Influence of prognostic factors on effectiveness
Measured: Complete observation time-frame (the total observation period of this study will amount to 90 months).
Prognostic factors
Influence of prognostic factors on safety
Measured: Complete observation time-frame (the total observation period of this study will amount to 90 months).
Treatment duration
From date of first treatment (encorafenib or binimetinib, whichever occurs first) until date of last treatment (encorafenib or binimetinib, whichever occurs last)
Measured: From start to end of treatment (anticipated median treatment duration ca. 12 months)
Treatment dose intensity
From date of first treatment (encorafenib or binimetinib, whichever occurs first) until date of last treatment (encorafenib or binimetinib, whichever occurs last)
Measured: From start to end of treatment (anticipated median treatment duration ca. 12 months)
Number of treatment interruptions
From date of first treatment (encorafenib or binimetinib, whichever occurs first) until date of last treatment (encorafenib or binimetinib, whichever occurs last)
Measured: From start to end of treatment (anticipated median treatment duration ca. 12 months)
Duration of treatment interruptions
From date of first treatment (encorafenib or binimetinib, whichever occurs first) until date of last treatment (encorafenib or binimetinib, whichever occurs last)
Measured: From start to end of treatment (anticipated median treatment duration ca. 12 months)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted5 Aug 2019
- Study start17 Oct 2019
- Primary completionDec 2026 (estimated)
- Study completionSep 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Melanoma Stage IVStudies 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
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 750 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Pierre Fabre Pharma GmbH
- Sponsor type
- Industry (pharma, biotech, devices)
- Collaborators
- Pierre Fabre Pharma Austria, Pierre Fabre Pharma AG
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04045691
- Sponsor's protocol ID
- NIS-PFO-2019-1921
- Acronym
- BERING
- Status last verified
- Jan 2021
- First submitted
- 25 Jul 2019
- Last updated
- 19 Jan 2021
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 19 Jan 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Encorafenib Plus Binimetinib in Patients With Locally Advanced, Unresectable or Metastatic BRAFV600-mutated Melanoma: a Multi-centric, Multinational, Prospective, Longitudinal, Non-interventional Study in Germany, Austria and Switzerland - BERING MELANOMA
- ClinicalTrials.gov ID
- NCT04045691
- Acronym / sponsor ID
- BERING / NIS-PFO-2019-1921
- Conditions
- Melanoma Stage IV, Melanoma Stage III
- Keywords
- BERING, Encorafenib, Binimetinib
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 750 participants (estimated)
- Lead sponsor
- Pierre Fabre Pharma GmbHIndustry (pharma, biotech, devices)
- Collaborators
- Pierre Fabre Pharma Austria, Pierre Fabre Pharma AG
- Study start
- 17 Oct 2019 (actual)
- Primary completion
- Dec 2026 (estimated)
- Study completion
- Sep 2027 (estimated)
- First posted
- 5 Aug 2019 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
BERING-MELANOMA - designed as a prospective, longitudinal, non-interventional study - investigates real-world effectiveness, quality of life, safety and tolerability of encorafenib plus binimetinib in unresectable advanced or metastatic BRAF(Rapidly Accelerated Fibrosarcoma isoform B)-V600-mutant malignant melanoma after commercial availability of these two products in Germany, Austria and Switzerland. The study focusses on the documentation of the first and second line setting (i.e. after one line of prior checkpoint inhibition) by documenting patients treated according to the SmPC (Summary of Product Characteristics).
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Adult patients with unresectable advanced or metastatic BRAFV600-mutant malignant melanoma, with a decision to receive targeted treatment with Encorafenib/Binimetinib according to the current SmPC.
Key inclusion criteria (6 listed)
- Written informed consent of the patient with regard to the pseudonymized documentation as well as the transfer and processing of his/her data within the study and the ADOREG [Cancer Registry of German Working Group of Dermato-Oncology] registry (data transfer to ADOREG registry only for patients from German sites);
- Legally capable male or female patient ≥ 18 years of age (no upper limit);
- Decision was taken to treat the patient with encorafenib plus binimetinib in accordance with the current SmPC [Summary of Product Characteristics] and by prescription; this decision was taken prior to and independent from the inclusion into the study;
- Treatment with encorafenib plus binimetinib has been started ≤ 6 months prior to providing written informed consent for this study or is planned to be started in the near future;
- Unresectable advanced or metastatic malignant melanoma with BRAF [Rapidly Accelerated Fibrosarcoma isoform B] V600 mutation;
Key exclusion criteria (8 listed)
- Previous treatment with a BRAF- and/or MEK [Mitogen-Activated Protein/Extracellular-signal Regulated Kinase]- inhibitor except for:
- -- prior adjuvant treatment with BRAF+MEK-inhibitor combination therapy that ended > 6 months prior start of Encorafenib/Binimetinib treatment;
- More than one prior line of checkpoint inhibitor treatment in the unresectable advanced or metastatic setting;
- Any previous chemotherapeutic treatment of the melanoma disease;
- Presence of any contraindication with regard to the encorafenib-binimetinib-treatment as specified in the corresponding SmPCs;
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 |
|---|---|---|
| EncorafenibObservation of real-life treatment with encorafenib and binimetinib | Drug | – |
| BinimetinibObservation of real-life treatment with encorafenib and binimetinib | Drug | – |
Primary outcome
Progression-free survival
Time frame: At 12 months after start of treatment
Progression-free survival rate
24 secondary outcomes
Patient and disease profiles at start of treatment with encorafenib plus binimetinib
Time frame: Baseline
Type of treatments before and after encorafenib plus binimetinib
Time frame: Complete observation time-frame (the total observation period of this study will amount to 90 months).
Sequence of treatments before and after encorafenib plus binimetinib
Time frame: Complete observation time-frame (the total observation period of this study will amount to 90 months).
Characteristics of treatment with encorafenib plus binimetinib
Time frame: From start to end of treatment (anticipated median treatment duration ca. 12 months)
Effectiveness of treatment with encorafenib plus binimetinib
Time frame: From start to end of treatment (anticipated median treatment duration ca. 12 months)
Effectiveness of treatment with encorafenib plus binimetinib
Time frame: From start to end of treatment (anticipated median treatment duration ca. 12 months)
Effectiveness of treatment with encorafenib plus binimetinib
Time frame: From start to end of treatment (anticipated median treatment duration ca. 12 months)
Effectiveness of treatment with encorafenib plus binimetinib
Time frame: From start to end of treatment (anticipated median treatment duration ca. 12 months)
Effectiveness of treatment with encorafenib plus binimetinib
Time frame: From start to end of treatment (anticipated median treatment duration ca. 12 months)
Effectiveness of treatment with encorafenib plus binimetinib
Time frame: From start to end of treatment (anticipated median treatment duration ca. 12 months)
Effectiveness of treatment with encorafenib plus binimetinib
Time frame: From start to end of treatment (anticipated median treatment duration ca. 12 months)
Effectiveness of treatment with encorafenib plus binimetinib
Time frame: Complete observation time-frame (the total observation period of this study will amount to 90 months).
Patient reported outcomes during treatment with encorafenib plus binimetinib - evaluated with EORTC QLQ C-30
Time frame: From start to end of treatment (anticipated median treatment duration ca. 12 months)
Patient reported outcomes during treatment with encorafenib plus binimetinib evaluated with WPAI
Time frame: From start to end of treatment (anticipated median treatment duration ca. 12 months)
Patient reported outcomes during treatment with encorafenib plus binimetinib evaluated with CTSQ
Time frame: From start to end of treatment (anticipated median treatment duration ca. 12 months)
Physicians' satisfaction with regard the treatment with encorafenib plus binimetinib
Time frame: From start to end of treatment (anticipated median treatment duration ca. 12 months)
Safety and tolerability of treatment with encorafenib plus binimetinib - Adverse events and adverse reactions including time to onset and time to resolution
Time frame: Complete observation time-frame (the total observation period of this study will amount to 90 months).
Prognostic factors
Time frame: Complete observation time-frame (the total observation period of this study will amount to 90 months).
Prognostic factors
Time frame: Complete observation time-frame (the total observation period of this study will amount to 90 months).
Prognostic factors
Time frame: Complete observation time-frame (the total observation period of this study will amount to 90 months).
Treatment duration
Time frame: From start to end of treatment (anticipated median treatment duration ca. 12 months)
Treatment dose intensity
Time frame: From start to end of treatment (anticipated median treatment duration ca. 12 months)
Number of treatment interruptions
Time frame: From start to end of treatment (anticipated median treatment duration ca. 12 months)
Duration of treatment interruptions
Time frame: From start to end of treatment (anticipated median treatment duration ca. 12 months)
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 19 Jan 2021.
- Individual participant dataSharing planned: No
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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.
59 sites in 3 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Melanoma Stage IV and Melanoma Stage III, run by Pierre Fabre Pharma GmbH at 59 sites in 3 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 6 inclusion and 8 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: looking for participants now, as of the sponsor's last update on 19 Jan 2021. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 59 sites in Germany, Austria, Switzerland. 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.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Christian A Rosé, MD (+49 761 45261 ext. 0, bering_de@pierre-fabre.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Progression-free survival (time frame: At 12 months after start of treatment). 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 19 Jan 2021.