Efficacy of JAK STAT Pathways Inhibitors in Treatment of Patients With Rheumatoid Arthritis

Sponsor
Adel A.Gomaa (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05788705
Collaborator
(none)
75
3
29

Study Details

Study Description

Brief Summary

There is no treatment that could utterly cure Rheumatoid arthritis (RA), but the disease is mainly improved by conventional disease-modifying anti rheumatic drugs. Methotrexate and biological DMARDs as JAK-STAT inhibitors may be used to control and delay the progression of the disease and improve the quality of lives of patients. However, DMARDs have deleterious effects on human health. Several natural components have JAK-STAT inhibitory effect such as Boswellic acid (Boswellia serrata extract), Glycyrrhizin (Glycyrrhiza glabra extr.) and Apigenin (Chamomile extr)

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: "apigenin" and "glycyrrhizin"
  • Dietary Supplement: "glycyrrhizin" and "boswellic acid"
  • Dietary Supplement: "placebo"
N/A

Detailed Description

Rheumatoid arthritis (RA) is a systemic chronic, progressive, autoimmune disease characterized by inflammatory cell infiltration and synovial proliferation, accompanied by injury to articular cartilage and subchondral bone The prevalence of RA in women is 3.6% and 1.7% for men . There is no treatment that could utterly cure RA, but the disease is mainly improved by conventional disease-modifying antirheumatic drugs. Methotrexate and biological DMARDs as JAK-STAT inhibitors may be used to control and delay the progression of the disease and improve the quality of lives of patients. However, DMARDs have deleterious effects on human health. Chronic use of these agents by pregnant patients may induce teratogenic effects . Many studies showed that some natural plant extracts or mixed herbal compounds effectively regulate the immune system and possess in vitro and/or in vivo inhibitory effects against STAT to alleviate RA by inhibiting pro-inflammatory cytokines. Several natural components have JAK-STAT inhibitory effect such as Boswellic acid (Boswellia serrata extract), Glycyrrhizin (Glycyrrhiza glabra extr.) and Apigenin (Chamomile extr.). Boswellic acid and its derivative acetyl-11- keto boswellic acid, are reported to be the most potent inhibitors in the synthesis of 5-LOX. Since 5-LOX is an important enzyme involved in the biosynthesis of leukotrienes and is significantly expressed in RA. B. serrata extract, when administered orally, inhibits IL-6, IL-1 , IFN- TNF- and PGE2 in complete Freund's adjuvant-induced arthritis in rats. Glycyrrhizin reduced the activity of JAK/STAT signaling pathway, which is the upstream regulator of HMGB1. These natural products have inhibitory effect for the STAT3 signaling pathway that have anti-inflammatory and anti-rheumatoid as well as anticancer effects. These inhibitors have been found to inhibit the STAT3 signaling pathway by reducing IL-6 production . Apigenin is a plant-derived flavonoid that is abundant in celery, Chamomile, plantain seed, and is effective in the prevention and treatment of inflammatory diseases, prostate cancer, and in inhibiting tumorigenesis and angiogenesis in melanoma, breast, skin, and colon cancers. Apigenin reduced p-JAK1/2 and p-STAT3 in breast cancer (BT-474) cells, and demonstrated antirheumatic and anticancer activity by inhibiting JAK-STAT . our aim To assess the efficacy of some natural JAK-STAT inhibitors as complementary medicine in the treatment of rheumatoid arthritis and attenuation of the side effects of regular methotrexate our Research outcome measures:

  1. Primary (main):

  2. The change in DAS28 based on C-reactive protein (DAS28-CRP) and the Clinical Disease Activity Index (CDAI)

  3. Rate of achieving 20%, 50% and 70% improvement in the American College Rheumatology criteria (ACR20, ACR50, ACR70).

  4. Secondary (subsidiary):

  5. Change in visual analogue scale (VAS).

  6. Determination of effusion synovitis volume on musculoskeletal ultrasound(MSUS)

  7. Determination of Inflammatory cytokines levels: (Tumour necrosis factor α and Interleukin 6).

  8. Safety and Tolerability Measures: adverse events including nausea, vomiting, dizziness and abdominal pain, CBC and urine analysis as well as kidney and liver function tests will be performed before enrolment.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
75 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Evaluation of the Efficacy of Natural JAK_ STAT Pathways Inhibitors in Treatment of Patients With Rheumatoid Arthritis as a Complementary Medicine
Anticipated Study Start Date :
Jul 1, 2023
Anticipated Primary Completion Date :
Jul 1, 2025
Anticipated Study Completion Date :
Dec 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: "apigenin" and "glycyrrhizin"

Patients will receive one capsule contains 10 mg of apigenin (Matricaria chamomilla L extract) and one capsule contains glycyrrhizin 50(licorice extract) twice daily for 6 months

Dietary Supplement: "apigenin" and "glycyrrhizin"
"apigenin" will be administered as capsule (10mg,eq 200mg Matricaria chamomilla L extract) two times daily. Also, "glycyrrhizin " will be administered as capsule(50 mg eq 250 mg licorice extract) two times daily. The two types of capsules administration will be continue for 6 months

Active Comparator: "boswellic acid" and "glycyrrhizin"

Patients will receive one capsule contains 200 mg boswellic acid (Boswellia serrata extract) and one capsule contains glycyrrhizin 50(licorice extract) twice daily for 6 months

Dietary Supplement: "glycyrrhizin" and "boswellic acid"
"boswellic acid" will be administered as capsule (200mg,eq 250mg Boswellia serrata extract) two times daily. Also, "glycyrrhizin " will be administered as capsule(50 mg eq 250 mg licorice extract) two times daily. The two types of capsules administration will be continue for 6 months

Placebo Comparator: "placebo"

Patients will receive daily two capsules contain placebo for 6 months

Dietary Supplement: "placebo"
"Placebo "capsule will be administered two times daily for 6 months

Outcome Measures

Primary Outcome Measures

  1. The change in DAS28 based on C-reactive protein (DAS28-CRP) [Before the intervention, 3 months after the intervention, and 6 months after the intervention]

    DAS-28 score: a DAS-28 score > 5.1 indicating high disease activity; 3.2< DAS-28 score≤5.1 indicates moderate disease activity; 2.6< DAS-28 score≤3.2 indicates low disease activity; DAS-28 score≤2.6 indicates basic disease remission

Secondary Outcome Measures

  1. Change in visual analogue scale (VAS [Before the intervention, 3 months after the intervention, and 6 months after the intervention]

    each patient will be asked to indicate his or her current level of pain on 100mm scale.0scale indicate no pain and 100mm indicate worst pain imaginable

  2. Determination of effusion synovitis volume on musculoskeletal ultrasound(MSUS) [Before the intervention, 3 months after the intervention, and 6 months after the intervention]

    Determination of effusion synovitis volume on musculoskeletal ultrasound

  3. Determination of Inflammatory cytokines levels: (Tumour necrosis factor α and Interleukin 6). [Before the intervention, 3 months after the intervention, and 6 months after the intervention]

    laboratory test

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Male or female,ages18-60.

  • Patients who met criteria for the diagnosis of RA

  • Patients who were signed the informed consent form.

Exclusion Criteria:
  • Patients with Malignant tumours,

  • Patients with Infectious diseases,

  • Patients with Hematologic diseases.

  • Patients with other rheumatic diseases.

  • Women who are pregnant or breastfeeding.

  • Hypersensitivity to dietary supplement used in this study.

  • Hypertensive patients

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Adel A.Gomaa

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Adel A.Gomaa, PROF OF CLINICAL PHARMACOLOGY, Assiut University
ClinicalTrials.gov Identifier:
NCT05788705
Other Study ID Numbers:
  • Natural JAK STAT Inhibitors
First Posted:
Mar 29, 2023
Last Update Posted:
Mar 29, 2023
Last Verified:
Mar 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 29, 2023