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Comparison of treatment efficacy in the patients with Systemic sclerOsis: dapagliFlozin vs. Tocilizumab – a randomized head to head study

Status
Withdrawn
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2025-523714-92-00
Acronym
2025-ABM-CMKP-01
Enrollment
80
Registered
2025-12-15
Start date
Unknown
Completion date
Unknown
Last updated
2025-12-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Systemic Sclerosis

Brief summary

Change in disease severity in both arms assessed using the modified Rodnan Scale (mRSS) after 12 months of therapy. Non-inferiority assumption: the difference in improvement (reduction) between the study arms does not exceed 3 points.

Detailed description

Change in the systemic sclerosis severity score for dapagliflozin compared to tocilizumab after 12 months of therapy. Superiority assumption: the difference in improvement (reduction) between the study arms exceeds 3 points in favor of dapagliflozin., Results of capillaroscopic examination according to the Cutolo scale after 12 months of therapy., Results of cardiac functional and morphological parameters assessed by magnetic resonance imaging (MRI) and echocardiography after 12 months of therapy., Results of morphological parameters of lung aeration on high-resolution computed tomography (HRCT) of the chest after 12 months of therapy., Results of renal function parameters (eGFR, albuminuria) after 12 months of therapy., Results of proinflammatory cytokine concentrations after 12 months of therapy., Results of a questionnaire developed by prof. Wioletta Tuszyńska-Bogucka, PhD, and standardized tools: the SF-36 Questionnaire, Pol-SScQoL Questionnaire (a scale designed to assess the quality of life of SSc patients), the Stress Assessment Questionnaire (KOS) by Wrześniewski et al., the Goldberg General Health Questionnaire (GHQ) in the Polish adaptation by Makowska and Merecz, the PHQ-9 Depression Scale, and the GAD-7 (Generalized Anxiety Disorder 7-item Scale) after 12 months of therapy., Safety assessment of the therapies used will include an analysis of the occurrence and characteristics of adverse events and serious adverse events during the study.

Interventions

DRUG9% FRESENIUS
DRUGRoActemra 20 mg/mL concentrate for solution for infusion
DRUGForxiga 10 mg film-coated tablets
DRUGPlacebo dapagliflozyny

Sponsors

Centrum Medyczne Ksztalcenia Podyplomowego
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Change in disease severity in both arms assessed using the modified Rodnan Scale (mRSS) after 12 months of therapy. Non-inferiority assumption: the difference in improvement (reduction) between the study arms does not exceed 3 points.

Secondary

MeasureTime frame
Change in the systemic sclerosis severity score for dapagliflozin compared to tocilizumab after 12 months of therapy. Superiority assumption: the difference in improvement (reduction) between the study arms exceeds 3 points in favor of dapagliflozin., Results of capillaroscopic examination according to the Cutolo scale after 12 months of therapy., Results of cardiac functional and morphological parameters assessed by magnetic resonance imaging (MRI) and echocardiography after 12 months of therapy., Results of morphological parameters of lung aeration on high-resolution computed tomography (HRCT) of the chest after 12 months of therapy., Results of renal function parameters (eGFR, albuminuria) after 12 months of therapy., Results of proinflammatory cytokine concentrations after 12 months of therapy., Results of a questionnaire developed by prof. Wioletta Tuszyńska-Bogucka, PhD, and standardized tools: the SF-36 Questionnaire, Pol-SScQoL Questionnaire (a scale designed to assess the qu

Countries

Poland

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026