Topical Dapsone 5% Gel versus Clindamycin 1% Gel in Mild-to-Moderate Acne Vulgaris

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24 Aug, 26

 

Introduction

Acne vulgaris is a highly prevalent inflammatory skin disease affecting adolescents and adults, often causing significant psychosocial burden. Topical clindamycin 1% is an established treatment; however, rising antibiotic resistance has created a need for alternative therapies. Dapsone 5% gel possesses both antimicrobial and anti-inflammatory properties and may offer effective acne control with minimal systemic exposure.

Aim

  • To compare the efficacy and safety of topical dapsone 5% gel versus topical clindamycin 1% gel in patients with mild-to-moderate facial acne vulgaris. 

Patient Profile

  • Patients with facial acne vulgaris
  • Aged 14-40 years 
  • Investigator's Static Global Assessment (ISGA) score ≥1 and <4

Methods

  • Prospective, randomized, double-blind clinical trial. 
  • Total 80 patients (40 per treatment group) were enrolled 
    • Group 1: Topical clindamycin 1% gel
    • Group 2: Topical dapsone 5% gel
  • Treatment duration: 12 weeks with once-daily nighttime application 
  • Efficacy assessments
    • ISGA         scores at baseline and at 4, 8, and 12 weeks

Grade

Clinical Description

0

Clear skin, no acne lesions

1

Nearly clear skin, few lesions

2

Mild acne with several comedones and few inflammatory lesions

3

Moderate acne with numerous lesions and few nodules

4

Severe acne with many inflammatory lesions including nodules

 

  1. Total Lesion Count (TLC) : Counts of comedones, papules, and pustules at baseline to 4, 8, and 12 weeks

Reduction in TLC

Response Category

<25%

Mild improvement

25-50%

Moderate improvement

51-75%

Significant improvement

>75%

Excellent improvement

 

  • Safety assessment included Adverse Drug Reactions (ADRs) 
  • Quality of life assessment: Cardiff Acne Disability Index (CADI) 

Results

  • 75 patients (37 in clindamycin group, 38 in dapsone group) completed the study
  • Both treatments significantly improved acne severity over 12 weeks, with comparable reductions in ISGA scores and total lesion counts at all follow-up points (4, 8, and 12 weeks), the differences between groups were not statistically significant (p>0.05), and both groups showed consistent improvement over time.
  • By 12 weeks, ISGA scores were comparable (Table 1)

Table 1. ISGA Score Improvement

Time Point

Clindamycin 1%

(Mean)

Dapsone 5%

(Mean)

p Value

Baseline

2.81 

2.65 

0.003

Week 4

2.32 

2.50 

0.465

Week 8

1.78 

1.55 

0.683

Week 12

1.189 

1.184 

0.913

 

  • Both groups achieved substantial reductions in total lesion count, with no significant difference between treatments (p = 0.148)
  • Reduction in non-inflammatory lesions (comedones) was similar in both groups
  • Topical dapsone demonstrated significantly greater effectiveness in reducing inflammatory lesions. Group 2 consistently showed a more pronounced reduction in papules from 4 weeks onward, with a notably lower mean count at 12 weeks (p=0.001). Similarly, pustule counts were significantly lower in group 2 at all follow-up points.

Table 2: Mean of Inflammatory Lesion Reduction During the Study Period

Lesion Type

Treatment 

Baseline

Week 4

Week 8

Week 12

p Value (Week 12)

Comedones 

Clindamycin 1%

14.32

9.72

6.40

4.43

0.941

Dapsone 5%

14.26

9.15

5.76

4.07

Papules 

 

Clindamycin 1%)

27.67

8.45

5.86

4.97

0.001

Dapsone 5%

28.97

10.26

8.15

0.65

Pustules 

Clindamycin 1%

4.56

2.05

0.20

1.91

<0.001

Dapsone 5%

3.18

0.52

0.63

0.65

 

  • Excellent TLC reduction (>75%) achieved in 43.2% of clindamycin-treated patients and 68.4% of dapsone-treated patients.

Table 3. TLC reduction at Week 12

 

Percentage of patients 

Response Category

Clindamycin 

Dapsone

Mild improvement (<25% reduction)

0

0

Moderate improvement (25-50% reduction)

0

0

Significant improvement (51-75% reduction)

56.7%

31.6%

Excellent improvement (>75% reduction)

43.2%

68.4%

 

Safety 

  • In Clindamycin Group40.54% of patients reported adverse drug reaction of which Erythema was the most frequently observed.
  • In Dapsone Group,50% of patients reported ADR. Dryness and irritation were the predominant side effects.
  • Dapsone showed a significant improvement in CADIscores at 12 weeks, with outcomes comparable to clindamycin (p = 0.213).

Conclusion

  • Topical dapsone 5% gel demonstrated efficacy comparable to topical clindamycin 1% gel for mild-to-moderate acne vulgaris.
  • Dapsone provided superior reduction of inflammatory lesions while maintaining a similar safety profile and improving quality of life. 

Reference

Int J Basic Clin Pharmacol. 2025;14(5):733-738.