31 Oct

The use of avodart with male pattern baldness

SUMMARY

1. The treatment of androgenetic alopecia is not an FDA-approved indication for Avodart (dutasteride). Therefore, Glaxo Smith Kline may not make recommendations on the use of Avodart for the purpose.
2. Avodart inhibits the conversion of testosterone to dihydrotestosterone (DHT) resulting in decreased serum DHT concentrations. By this mechanism, Avodart appears to interrupt a key process in the development of androgenetic alopecia (AGA), also known as male pattern hari loss (MPHL).
3. A phase II, multi-center double blind, placebo controlled study was conducted in 416 males with AGA, ages 21-45 years, to evaluate the dose response relationship of Avodart on hair growth. Repeated doses of Avodart (0.05mg), 0.5mg, and 2.5mg daily) were compared to placebo for 6 months. Safety and tolerability of the varying doses of Avodart and finasteride 5mg daily compared with placebo were also investigated.
4. A dose related increase in hair count was seen at week 12 and 24 in patients receiving Avodart, significant increases were also observed in the finasteride treatment group. The increase in hari count was maintained after the cessation of treatment aw=t week 36 (12 weeks after medication discontinuation) in the Avodart 0.5mg and 2.5mg treatment groups, but not in the finasteride or Avodart 0.05mg and 0.1mg treatment groups.
5. The most common drug-related adverse events were decreased libido experienced by 13% of subjects receiving Avodart 2.5mg/day, followed by headaches experienced by 8% of the Avodart 0.1mg/day group and 6% of the Avodart 0.5mg/day and 2.5mg/day group.
6. No large, prospective clinical trials have evaluated the use of avodart for AGA.
7. Avodart is indicated for the treatment of symptomatic benign prostatic hyperplasia (BPH) in men with an enlarged prostate to improve symptoms, reduce the risk of acute urinary retention, and reduce the risk of the need for BPH-related surgery. Avodart is contraindicated for use in women and children and for patients with known hypersensitivity to dutasteide, other 5?-reductase inhibitors, or any component of the preparation.

Some information contained in this response may be outside the approved prescribing information for Avodart . This response is not intended to offer recommendations for administerin Avodart in a manner inconsistent with its approved labeling. In order for Glaxo Smith Kline to monitor the safety of avodart, we encourage healthcare professionals to report adverse events or suspected overdoses to the company at 888-825-5249. Please consult the Prescribing Information for Avodart.

Background

Androgenetic alopecia (AGA), also known as male pattern hair loss (MPHL), is the most common form of hair loss, affecting approximately 50% of Caucasians over the age of 40 years (1). In males, AGA can begin as early as late adosescence; however, the usual onset is at around the age of 30 years (1). AGA results from naturally circulating androgens which progressively transform large terminal scalp follicles to smaller vellus ones, thus resulting in a visibly less dense scalp (2).

Testosterone is the major circulating androgen in the body, but must be converted to dihydrotestosterone (DHT) via the enzyme 5 a -reductase in order to be active in the skin (3). Studies have shown that men with 5 a -reductase deficiency do not develop AGA (*3,4). Therefore, 5 a -reductase inhibitors have been evaluated for the treatment of AGA due to their ability to inhibit the conversion of testosterone to dihydrotestosterone (3,5). Two iso forms of 5 a -reductase are known, type 1 and type 2. Type 2 is predominately located in human genital tissue. Type 1 is distributed throughout the body, and predominates in the skin and scalp (3).

Avodart is a competitive inhibitor of 5 a -reductase, the enzyme responsible for the conversion of testosterone eo dihydrotestosterone (DHT) in the prostate. It inhibits both enzyme types 1 and 2 and is indicated for the treatment of symptomatic BPH in men with an enlarged prostate to improve symptoms, reduce the risk of acute urinary retention, and reduce the risk of the need for BPH-related surgery. Avodart is contraindicated for use in women and children and for patients with known hypersensitivity to dutatsteride, other 5 a -reductase inhibitors, or any component of the preparation (6).

One clinical trial evaluating the use of Avodart in AGA has been conducted and is discussed below. No large, prospective clinical trials have evaluated the use of Avodart for this use.

Clinical information

A phase 2, multi-center, double blind, placebo-controlled study was conducted in 416 males with AGA, ages 21 to 45 year, to evaluate the dose response relationship of repeated doses of Avodart (0.05mg, 0.1mg,0.5mg, and2.5mg daily) on hair count compared to placebo for 6 months. Safety and tolerability of the varying doses of Avodart and finasteride 5mg daily compared with placebo were also investigated. At the time this study was conducted, the1-mg dosage strength of finasteride that is currently approved for the treatment of AGA was not available (7).

Patients were included in this study If they had MPHL defined as type IIIv,IV, or V by the modified Norwood-Hamilton classification and had active hair loss or progression in the size of the balding area withig the past 2 years.Patients were randomized into one of the following xix treatment groups:Avodart 0.05mg (n=71), Avodart 0.1mg (n=72), Avodart 0.5mg (n=71),finasteride 5mg (n=70), or placebo (n=64) (7). Patients received oral doses once daily for 24 weeks. The study also included and additional follow-up visit and evaluation of hair count at 36 weeks (12 weeks after double-blind study medication had been stopped) (7).

Efficacy was assessed by measuring hair counts of the vertex region of the scalp using macro photographic techniques at baseline, 12 weeks, 24 weeks, and at the follow-up visit at 36 weeks (12 weeks after study medication discontinuation). The primary efficacy parameter was the hair count in a 1-inch diameter circle, with a target area of 0.79 square inches,surrounding a tattoo. Results are presented in Table 1 and reflect last observation carried forward (LOCF) (weeks 12 and 24) or at the last visit (ALV)(week 36) analyses of the intent-to-treat population (7).

Table 1: Hair count: change from baseline using 0.79square inch target area

(Intent to Treat Population)*(7) 

Avodart

Time/Parameter

0.05mg/day

0.1mg/day

0.5mg/day

2.5mg/day

Finasteride

5mg/day

Placebo

Week 12

N

Mean *

Mean Difference **

p-value

 

61

5.0

27.9

0.065

 

65

54.3

77.2

<0.0001

 

59

71.9

94.8

<0.001

 

63

100.4

123.3

<0.001

 

68

52.1

75.0

<0.001

 

57

-22.9

-

-

Week 24

n

Mean*

Mean Difference**

p-value

 

62

24.8

54.4

<0.001

 

66

72.3

101.9

<0.001

 

63

95.5

125.1

<0.001

 

67

109.8

139.5

<0.001

 

69

73.2

102.8

<0.001

 

58

-29.6

-

-

Week 36

N

Mean*

Mean Difference**

p-value

 

47

-17.1

20.2

0.29

 

52

16.8

54.1

0.004

 

51

84.3

121.6

<0.001

 

54

119.8

157.1

<0.001

 

61

13.2

50.5

0.005

 

46

-37.3

-

-

which are reported as at last visit (ALV) values; * Adjusted for baseline values; ** difference between active treatment and placebo.]

As noted in Table 1, dose-related increases in hair count were seen at 12 and24 weeks across the Avodart treatment groups. Compared to placebo, these changes were significantly different in all Avodart treatment groups ( P <0.001) except for in the 0.05 group at week 12 ( P<0. 065).Hair count change from baseline in the finasteride group was also significantly greater than the placebo group at both 12 and 24 weeks ( P< 0.001)(7).

At week 36 (12 weeks after cessation of daily medication), improvement in hair count was maintained at similar level to that observed at week 24 in those patients receiving Avodart 0.5mg (35.5 at week 24 and 84.3 at week 36) and 2.5mg(109.9-8 at week 24 and 119.8 at week 36) daily. In contrast, improvement in hair count was not maintained in those patients receiving finasteride 5mg at week 36 compared to week 24 (73.2 at week 24 and 13.2 at week 36), Advodart 0.05mg (24.8 at week 24 and -17.1 at week 36), or Avodart 0.1mg (72.3 at week 24and 16.8 at week 36)(7).

Adverse Events

Twenty-five percent (102/416) of subjects experienced atotal of 169 adverse events that were classified by the investigator as having areasonable possibility of being drug-related (7). Those drug-related adverseevents having and incidence > 5% within any treatment group are presented inTale 2.

 

Table 2: Percent (%) of Subjects with Drug-RelatedAdverse Events

( > 5% of Subjects Within Any Treatment Group)

Avodart

Adverse Event

0.05mg/day N=71

0.1mg/day N=72

0.5mg/day

N=68
2.5mg/day

N=71

Finasteride 5mg/day N=70

Placebo

N=64

Any Adverse Event

18

29

16

32

24

27

Altered (Decreased)

Libido

3

3

0

13

4

3

Impotence

1

0

0

0

1

5

Headaches

1

8

6

6

3

3

Nausea and Vomiting

0

0

1

1

0

5

Malaise and Fatigue

1

1

1

7

3

3

Abnormal Liver

Function Tests

3

1

0

0

0

5

The most common drug-related adverse event were decreased libido experienced by 13% of subjects receiving Avodart 2.5 mg/day followed by headaches,experienced by 8% of the Avodart 0.1mg/day group and 6% by both the Avodart 0.5mg/day and 2.5 mg/day group. There were no serious adverse events that were considered drug-related.

Partner Pregnancies

Five partner pregnancies were reported during thestudy. One female partner spontaneously aborted (study subject was on placebo)and one had a partial placenta previa with subsequent delivery of a normal maleinfant (study subject was on Avodart 0.5 mg). The other three pregnancies weenormal and resulted in the births of two males (two subjects on "Avodart 0.5mgand one on Avodart 2.5mg) and one female (subject on Avodart 2.5mg). None of theinfants had genital or other abnormalities at birth (7).

Precaution

Avodart Soft Gelatin Capsules should not be handled by awoman who is pregnant or who may become pregnant because of the potential forabsorption of dutasteride and the subsequent potential risk to a developing malefetus. Avodart is contraindicated for use in women. Avodart has not been studiedin women because preclinical data suggest that the suppression of circulationlevles of dihydrotestosterone may inhibit the development of the externalgenital organs in a male fetus carried by a woman exposed to dutasteride (6) REV0704

REFERENCES

•  Meidan VM, Touitou E. Treatments for androgenetic alopecia and alopecia areata: current options and future prospects. Drugs 2001;61:53-69.

•  Randall VA. Physiology and Pathophysiology of Androgenetic Alopecia. In:Endocrinology, 4 th ed. Volum 3. DeGrrot LJ and Jameson JL (editors). W.B.Saunders Co, Philadelphia PA, 2001,pages 2257-2268.

•  Rittmaster RS. Clinical relevance of testosterone and dihydortestosterone metabolism in women. Am J Med 1995;98 (Suppl 1A): 17S-21S.

•  Wilson Jd, Griffin Je, Russell DW. Steroid 5 alpha-reductale 2 deficiency.Endocr Rev 1993;13:1-14.

•  Rittmaster RS. Finasteride. N. Engl J Med 1994;330:120-125.

•  Prescribing Information for Avodart Ô .

•  Data on file (Dutasteride, GM2000/00244/00, Study ARIA2004 Report Synopsis, 2001).

Enclosures: Product Information for Avodart Ô

 

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