Clinical Trial: A Pooled Analysis of the HGS1006-C1056 (BLISS-52) and HGS1006-C1057 (BLISS-76) Studies

Study Status: Completed
Recruit Status: Completed
Study Type: Observational

Official Title: Efficacy and Safety of Belimumab in a Subgroup of Systemic Lupus Erythematosus (SLE) Patients With Higher Disease Activity (Anti-dsDNA Positive and Low Complement): A Pooled Analysis of the HGS1006-C1

Brief Summary: Efficacy and Safety of Belimumab in a Subgroup of Systemic Lupus Erythematosus (SLE) Patients with Higher Disease Activity (anti-dsDNA positive and low complement): A Pooled Analysis of the HGS1006-C1056 (BLISS-52) and HGS1006-C1057 (BLISS-76) Studies

Detailed Summary:

Studies C1056 and C1057 followed very similar protocols, were of nearly identical design, had common inclusion and exclusion criteria, and were conducted over the same time period. Nevertheless, given the heterogeneous presentation of SLE disease and the fact that the Phase III program was run globally, variation in the patient population, both within the studies (e.g., between different centres) and between the studies (analogous to differences between centres within the same study) should be expected.

Since it has been established that the conduct of the studies was effectively the same, it then must be determined whether the relative treatment effect is different in one study compared with the other study when evaluating whether two studies are similar enough to pool. Each of these Phase III studies achieved statistical significance for belimumab 10 mg/kg on the pre-specified primary endpoint of SRI response at Week 52; therefore, these nearly identical studies provide independent replication of results. While pooling is not necessary to establish the effectiveness of belimumab, it was considered appropriate in order to evaluate treatment effects in the high disease activity subgroup of interest, given that the individual studies were not designed to provide sufficient power to demonstrate effectiveness within subgroups. Thus, statistical evaluation pooling the studies and testing for a treatment-by-study interaction was undertaken. A significant treatment-by-study interaction would indicate that the relative treatment differences were statistically different in the two studies and pooling would not be justified. Conversely, the lack of a treatment-by-study interaction would indicate the studies resulted in a similar treatment response and pooling would be justified.

When the two Phase III studies were pooled for the SR
Sponsor: Human Genome Sciences Inc., a GSK Company

Current Primary Outcome: SLE (systemic lupus erythematosus) Response Index (SRI) at Week 52 [ Time Frame: Response rate by visit through Week 52 for the pooled studies and through Week 76 for Study C1056 ]

Composite endpoint resulting from the combination of three well-established tools for evaluating SLE disease activity which include an objective measure of the reduction in global disease activity for efficacy and two measures to ensure that the improvement in disease activity (score) is not offset by worsening of the subject's condition overall.


Original Primary Outcome: Same as current

Current Secondary Outcome:

  • The response rate by visit modified to exclude anti-dsDNA and complement items in the determination of a 4-point reduction in SELENA SLEDAI (Safety of Oestrogen in Lupus National Assessment Systemic Lupus Erythematosus Disease Activity Index). [ Time Frame: By visit up to Week 52 for pooled studies. ]
  • The percent of subjects with no new BILAG A (British Isles Lupus Assessment Group) organ domain score or 2 new BILAG B organ domain scores [ Time Frame: By visit up to Week 52 for pooled studies ]
  • Percent of subjects with greater than 4 point reduction from baseline in SELENA SLEDAI (Safety of Oestrogen in Lupus National Assessment Systemic Lupus Erythematosus Disease Activity Index) [ Time Frame: By visit up to Week 52 ]
  • Mean change in PGA (Physician's Global Assessment) [ Time Frame: At Week 24, and by visit up to week 52 (population a only). ]
  • All Flares and Severe Flares will be assessed for population a [ Time Frame: In periods of Weeks 0-52 and weeks 24-52 ]
    Number of subjects experiencing a flare/severe flare (Weeks 0-52 and Weeks 24-52). Time to 1st flare/severe flare (Weeks 0-52 and Weeks 24-52.) Flares/Severe flares per subject year (Weeks 0-52).
  • All BILAG A (British Isles Lupus Assessment Group) Flares will be assessed for population a [ Time Frame: In periods of Weeks 0-52 and Weeks 24-52 ]
    Number of subjects experiencing a BILAG A flare (Weeks 0-52 and Weeks 24-52). Time to 1st BILAG A flare (Weeks 0-52 and Weeks 24-52). BILAG A flares per subject year (Weeks 0-52).
  • Percent of Subjects with Daily Prednisone Dose Reduced to ≤ 7.5 mg/day from > 7.5 mg/day at Baseline by Visit [ Time Frame: For pooled studies through Week 52 ]
  • Mean change in SF-36 (Short Form 36 Health Survey questionnaire) domains (population a only), Physical Component Summary (PCS) and Mental Component Summary MCS (population a only) [ Time Frame: By visit up to Week 52 ]
  • Mean change in FACIT (Functional Assessment of Chronic Illness Therapy) Fatigue Scale score [ Time Frame: By visit up to Week 52 ]
  • EQ-5D (EuroQol five dimension self-reported health state questionnaire) individual item score (mobility, self-care, usual activities, pain/discomfort, anxiety/depression) [ Time Frame: Change from baseline by visit up to Week 52 ]
  • Improvement in each SELENA SLEDAI (Safety of Oestrogen in Lupus National Assessment Systemic Lupus Erythematosus Disease Activity Index) organ domain [ Time Frame: At week 52 ]
  • Percent of subjects with no worsening in PGA (Physician's Global Assessment) [ Time Frame: By visit up to Week 52 ]
  • Percent of Subjects with Daily Prednisone Dose Increased to > 7.5 mg/day from ≤7.5 mg/day at Baseline by Visit [ Time Frame: For pooled studies through Week 52. ]
  • Percent of Subjects with Daily Prednisone Dose Reduced by ≥25% and to ≤ 7.5 mg/day from > 7.5 mg/day at Baseline by Visit [ Time Frame: For pooled studies through Week 52 ]
  • Time to first SELENA SLEDAI (Safety of Oestrogen in Lupus National Assessment Systemic Lupus Erythematosus Disease Activity Index) organ improvement by organ domain, among subjects with involvement at baseline [ Time Frame: Over Weeks 0-52 ]
  • Time to first BILAG organ improvement by organ domain, among subjects with involvement at baseline [ Time Frame: Over Weeks 0-52 ]
  • EQ-5D (EuroQol five dimension self-reported health state questionnaire) index score using value set for the UK [ Time Frame: Change from baseline by visit up to Week 52 ]
  • EQ-5D (EuroQol five dimension self-reported health state questionnaire) visual analogue scale (VAS) score using value set for the UK [ Time Frame: Change from baseline by visit up to Week 52 ]
  • The response rate calculated without allowable and prohibited medication rules applied (population a only). [ Time Frame: By visit up to Week 52 ]


Original Secondary Outcome: Same as current

Information By: GlaxoSmithKline

Dates:
Date Received: December 19, 2012
Date Started: May 2011
Date Completion:
Last Updated: May 16, 2013
Last Verified: May 2013