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Efficacy and Safety Study of BDB-001 Injection in Patients With Moderate to Severe Hidradenitis Suppurativa (HS)

A Multicenter, Open-label, Phase II Study to Explore Efficacy and Safety of BDB-001 Injection in Subjects With Moderate to Severe Hidradenitis Suppurativa

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05093855
Enrollment
41
Registered
2021-10-26
Start date
2021-08-18
Completion date
2023-08-22
Last updated
2023-08-29

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

Conditions

Hidradenitis Suppurativa

Brief summary

The purpose of this study is to explore whether BDB-001 Injection is effective and safe in the treatment of moderate to severe hidradenitis suppurativa(HS).

Interventions

Multiple IV infusions of BDB-001 Injection diluted in sodium chloride

Sponsors

Staidson (Beijing) Biopharmaceuticals Co., Ltd
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Subjects who signed the informed consent to participate in the STS-BDB001-06 clinical study and completed all follow-up of the study as required by the protocol, or who withdrew early due to treatment failure or other objective reasons and completed the early withdrawal visit (at least 4 weeks of treatment)

Exclusion criteria

* Never participated in the clinical study of STS-BDB001-06; * Subjects withdrew from the STS-BDB001-06 clinical study due to an intolerable adverse event related to the study drug.

Design outcomes

Primary

MeasureTime frameDescription
Change in International Hidradenitis Suppurativa Severity Score System (IHS4) score from Day 0 by time pointWeek 8The International Hidradenitis Suppurativa Severity Score 4 (IHS4: developed by the European Hidradenitis Suppurativa Foundation Investigator Group),IHS4 Score=(Nodule Count) + (Abscess Count\*2) + (Draining Tunnel Count \*4). IHS4 score uses a range grades: Mild=0-3; Moderate=4-10; Severe ≥11.

Secondary

MeasureTime frameDescription
Change in International Hidradenitis Suppurativa Severity Score System (IHS4) score from Day 0 by time pointFrom Day 0 until Day 56The International Hidradenitis Suppurativa Severity Score 4 (IHS4: developed by the European Hidradenitis Suppurativa Foundation Investigator Group),IHS4 Score=(Nodule Count) + (Abscess Count\*2) + (Draining Tunnel Count \*4). IHS4 score uses a range grades: Mild=0-3; Moderate=4-10; Severe ≥11.
Change in modified Sartorius Score (mSS) from Day 0 by time pointFrom Day 0 until Day 56The mSS is a summation of HS lesions based on a number of factors including anatomical region, number and type of lesions, distance between relevant lesions and lesions clearly separated by normal skin in each region measured as HS clinical parameters. The scale title for mSS is points. The mSS has a minimum value of 0 and no upper limit. The higher the score the more severe is the disease/worse is the outcome.
Change in Hidradenitis Suppurativa Clinical Response (HiSCR) from Day 0 by time pointFrom Day 0 until Day 56The definition for response to treatment based on HiSCR relative to Baseline was: at least 50% reduction in abscesses and inflammatory nodule (AN) count (over all anatomical regions) with no increase in number of abscesses and in number of draining fistulas.
Safety of BDB-001 injection in the treatment of patients with HS will be assessedFrom Day 0 until Day 77Number of participants with treatment-related adverse events as assessed by CTCAE v5.0.
Changes of active lesions (number of inflammatory nodules, abscesses, fistulas, and abscess overflow score) from Day 0 by time point.From Day 0 until Day 56
Change in Dermatology Life Quality Index (DLQI) score from Day 0 by time pointFrom Day 0 until Day 56A score is documented for each of the 10 DLQI items, ranging from 0 to 3 for each item. The scale title for DLQI is points. The total score is the sum of the responses to all 10 DLQI items, ranging from the minimum of 0 points to the maximum of 30 points. A higher score corresponds to worse health related quality of life/outcome.
7. Change in Dermatology visual analog scale (VAS) score from Day 0 by time point.From Day 0 until Day 56]
Change in Hidradenitis suppurativa-Physician Global Assessment (HS-PGA) score from Day 0 by time pointFrom Day 0 until Day 56Hidradenitis Suppurativa - Physician's Global Assessment (HS-PGA)classifies patients' severity into six categories:clear, minimal, mild, moderate, severe, and very severe, based on the number and quality of inflammatory lesions.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026