CBD/THC Solution as a Pharmacological Strategy for Patients With Fibromyalgia. Single-center, Double-blind, Randomized, Placebo-controlled Clinical Trial Protocol (FibroCann)

Patients with fibromyalgia will be recruited from tertiary health care establishments, specifically patients treated in the area of rheumatology, for eligibility assessment according to inclusion and exclusion criteria by the rheumatologist participating in this study, Osvaldo Haider Jr (CRM- PR 22274). It is important to point out that the patients' participation in the study will be voluntary, with no expectation of remuneration of any kind. Recruitment for the two stages will follow these steps: The first recruitment, in tertiary health care centers, in the rheumatology specialty, will start after approval of this project by the ethics committee; Dissemination of the study will be carried out via social networks and direct dissemination to doctors and tertiary health care clinics, which serve the rheumatology specialty; Enrolled volunteers must attend the evaluation for the inclusion and exclusion criteria, which will be carried out at the 3F Clinical Trials research center in a reserved environment at the clinical research centers contracted by 3F Clinical Trials; Patients must come with a medical report attesting to the diagnosis of fibromyalgia; The clinical evaluation, to meet the inclusion and exclusion criteria, will be performed under the supervision of the Rheumatologist Principal Investigator (PI) of this study, Osvaldo Haider Jr (CRM-PR 22274). Assessments of clinical symptoms, history will be performed, and the patient will be referred for laboratory tests of renal and hepatic profile. Additionally, women of childbearing age will undergo a biochemical hCG test. Additional tests for diagnostic confirmation or confirmation of any inclusion and exclusion criteria from the study may be requested; If there is a need for analysis of exams or the patient's medical history, it will be formally requested to the tertiary care center, where the patient undergoes his regular treatment, according to the requirements of the place, and according to the data use term. on file, the data will be kept confidential; Patients who are able to participate in the study, according to a clinical rheumatological evaluation, will undergo a pharmaceutical evaluation, carried out by the pharmacist responsible for this study, Ma. Ana Carolina Martins (e-CRF-PR 29255), to analyze the criteria in relation to the previous use of Cannabis, drug interactions in conventional treatment, possible reports that may exclude the patient from the study; Being able to participate in the study, the selected patients must read the informed consent; Patients will be informed that the project is placebo-controlled, and that this allocation to active treatment or placebo is random and double-blind; Agreeing with the terms, the patient will sign the informed consent in two copies, one for him and another for the researcher. Participants will undergo a variety of examinations, questionnaires and tests during screening, enrollment and allocation, in-intervention assessments, final treatment assessment and for a post-trial period monitoring period. It is noteworthy that the evaluations performed through the clinical questionnaires established in this protocol will be made by telephone. The following tests and protocols will be used: Pregnancy Test and Vital Signs; Pain; Depression; Sleep; Quality of life; Adverse Effects Monitoring; Laboratory; Tests. The pre-randomization period will take place in weeks -8 to 0 in order to make sure that all participants meet all the inclusion criteria. Participants who are under pharmacological treatment must have their treatments stable for at least 60 days and not make changes to these treatments during the clinical trial, without such procedure being duly registered. Patients eligible for the study, following the inclusion and exclusion criteria, will be randomized in a 1:1:1:1 ratio to receive CBD/THC 1:1 (0.1 mg/ml) (n=10), CBD/THC 1:1 (1.0 mg/ml) (n=10), CBD/THC 1:1 (10 mg/ml) (n=10) or placebo (vehicle) (n=10), daily, once a day day. The treatment will have a total duration of 120 days. The dose was chosen based on preliminary results of pilot studies conducted by this research group (with unpublished results) and also according to the characteristics of the drug produced by the sponsor. In addition, evidence has shown that doses in previously published studies have doses within this range or even above the concentration determined for our study (see item 11.1). The clinical study will have a baseline assessment (T0), one day before the start of the intervention with the solution. The tools will be reapplied after 15 (T1), 30 (T2), 60 (T3), 90 (T4) and 120 (T5) days of intervention. Medical monitoring of vital signs and clinical evidence of potential adverse effects will take place throughout the study. In this trial, for ethical reasons, patients will not be advised to discontinue the pharmacological treatment currently in use (e.g., opioids, antidepressants, benzodiazepines, gabapentinoids, anti-inflammatory drugs, or other non-opioid analgesics). The CBD/THC solution will be administered to participants as an oral solution. The drug will be provided by the company FG Brasil LTDA, under the trade name Aura Pharma, which is a company that imports cannabinoid products and sponsors this study. The product consists of a solution containing the phytopharmaceuticals CBD and THC, both at a concentration of 10mg/mL. The dilution vehicle is MCT (medium chain triglycerides) oil. Product development is carried out at Schibano Pharma AG Tüfi, 450 - Wald Schönengrund - 9105, Switzerland, and is obtained under Good Manufacturing Practices (GMP) protocols, ensuring a level of pharmaceutical quality for human use, and free from the addition of isolated substances of synthetic or semi-synthetic origin. The sponsor will also provide the placebo, which consists of the vehicle without the addition of CBD and THC phytopharmaceuticals, maintaining the same organoleptic aspects of the CBD/THC solution. The solution will be provided by the study sponsor, packaged in 10 mL vials, along with a dosing syringe (with graduation lines) for oral administration. The patient will be instructed to store the bottle in a place with a temperature of up to 30°C, dry, protected from light and heat, and out of the reach of children. Dilution will be carried out in the same vehicle as the base drug, which will be provided by the sponsor, for doses of 0.1 and 1mg/ml. Thus, all patients will aspirate the equivalent volume to be administered (1mL/day) from their own bottle, corresponding to: (i) Group 1: 0.1mg of CBD and 0.1mg of THC; (ii) Group 2: 1mg of CBD and 1mg of THC; (iii) Group 3: 10mg of CBD and 10mg of THC; (iv) Group 4: placebo/vehicle. The time of administration will be daily, in the evening before going to bed, and 30 minutes after the meal. Participants will be instructed to wash the syringe with water and detergent after use, and rinse thoroughly with running water through repetitive aspirations. It should be noted that a double quality control will be carried out, with physical-chemical analysis, prior to the availability of the product for the study. The first quality review is carried out by the product developer in Switzerland. Finally, the second quality analysis is performed by Aura Pharma in Brazil. Labeling and storage: All study products will be labeled in English and Portuguese in accordance with local regulations for investigational drugs. A total of 40 patients will be required to detect a significant difference from treatment with the standardized CBD/THC solution. We performed an a priori calculation using the effect size described by Yanes et al. (2019) (Cohen's d = 0.58), considering an analysis of covariance (ANCOVA) design for repeated measures, alpha (α) set at 5% and statistical power (β) at 80%. In this case, we use the software GPower\* 3.1.9.7 (Heinrich-Heine-Universityät, Düsserldorf). The collection and preservation of clinical data complies with standard requirements for data management and handling in accordance with the ICH/BPC. A secure database will be established for the collection of clinical data through the e-CRF platform via a secure connection at clinical research facilities and with traceable restricted access. All data obtained during the study will be documented in the individual e-CRF. In case of missing data, the reasons for this will be noted in the e-CRF. Participant information collected in the e-CRF, but not recorded in the patient's files, will be considered as source documents. Patient participation and any treatment-related AE in the study will be documented in the e-CRF. No patient information, such as medical history and medication history, will be collected before the informed consent has been obtained from the patient. Information obtained directly from potential participants prior to obtaining the informed consent (ie, during eligibility screening) will be recorded in the e-CFR, and this information will be made available to researchers with the patients' permission. The study will end when the last patient completes the last clinical evaluation at the end of 120 days of treatment, or the patient may for some reason discontinue the intervention and choose to withdraw from the clinical trial. This protocol will be suspended or terminated if the Principal Investigator, in agreement with the research team: Perceive that there is a risk or harm to the health of voluntary participants, and this risk is directly associated with the investigational drug and not provided in the informed consent; observe the occurrence of a serious adverse event after signing the informed consent, which results in: 1) death; 2) threat or risk to life; 3) need for hospitalization; 4) prolongation of preexisting hospitalization; 5) permanent disability or damage; or 6) a significant medical occurrence that, based on appropriate medical judgment, may impair the participant's exclusion criteria and/or require medical or surgical intervention to prevent any of the other aforementioned occurrences. In case of termination or suspension of this study, all participants will be informed, receive appropriate therapy and be followed up by the responsible physician and research team.