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January 15, 2007
QuatRx announced positive results from a phase II trial of fispemifene for the treatment of androgen deficiency and related disorders in men. This randomized, double-blind, placebo-controlled trial enrolled 77 men with secondary hypogonadism, in the US. Subjects received 100, 200 and 300 mg doses of fispemifene or placebo for 28 days. Results revealed a 60%, 60% and 78% increase in testosterone levels for the 100, 200 and 300 mg fispemifene groups, respectively, while those on placebo showed a 14% increase in testosterone levels (p<0.05, p<0.01, p<0.001, respectively). In all dose-groups the mean testosterone level increased into the normal range of 300 ng/dL to 900 ng/dL. Based on the results, QuatRx plans to advance the development of fispemifene for the treatment of hormone deficiency.
September 18, 2006
Ardana announced positive preliminary results from a phase II trial of its testosterone cream for the treatment of male hypogonadism. This trial enrolled 16 men who were divided into 2 groups of 8 and randomized to receive a single daily application of testosterone cream at a dose of either 2.25g or 4.5g for 28 days. Testosterone concentrations were measured for 24 hours on the last day of the study, day 28. Preliminary efficacy analysis showed that 80% of the subjects on the lower dose treatment had testosterone levels with an average concentration of 4.74 ng/ml, well within the normal range of 3-10 ng/ml. This data indicates that only a small number of subjects would need the higher dose concentration of the cream to restore testosterone levels to the normal range. Additional phase I and II trials are ongoing and a phase III trial is being planned.
October 3, 2005
Altus Pharmaceuticals issued positive results of a phase I trial of their long-acting crystalline formulation of human growth hormone (HGH) ALTU-238, for the treatment of HGH deficiency, at the 7th joint meeting of the European Society for Paediatric Endocrinology and the Lawson Wilkins Pediatric Endocrine Society in Lyon, France. Trial data yielded pharmacokinetic and pharmacodynamic data supportive of once-weekly subcutaneous dosing, and a single-dose of the drug produced sustained serum IGF-1 levels comparable to 7 daily injections of an approved HGH formulation. This open-label study enrolled healthy adults, who received a single subcutaneous injection of the drug.
August 8, 2005
Auxilium reported top line results of a phase II trial of their androgen replacement transmucosal film, for the treatment of male hypogonadism. Preliminary data yielded evidence of efficacy, with 3 doses of the film each yielding increases in serum testosterone levels; the efficiency of absorption indicated that the lowest trial dose would be optimal for future studies. The film had a positive overall tolerability profile, and 97% of subjects indicated that the film treatment was "desirable" or "acceptable." This open-label study enrolled 69 hypogonalal men, who received daily applications of the film at one of three dose levels (5 mg, 10 mg or 15 mg).
March 21, 2005
GTx has reported positive results of a phase I trial of their non-steroidal selective androgen receptor modulator ostarine, for the treatment of andropause, sarcopenia, and other symptoms of testosterone deficiency. Trial data indicated that the drug was safe and well tolerated, with no serious dose-related or clinically significant adverse events observed. Pharmacokinetic data yielded a positive profile supportive of further development. This double-blind, placebo-controlled study enrolled 96 healthy volunteers, who received single ascending doses of the drug. The company, based on these results, announced plans to initiate a phase I multiple ascending dose study of the drug in April 2005.
September 20, 2004
Auxilium Pharmaceuticals has reported the results of a phase IV study of their topical testosterone therapy Testim, for the treatment of hypogonadism in men unable to achieve symptom amelioration with AndroGel, another topical testosterone therapeutic. The study found that Testim therapy was effective in treating symptoms of hypogonadism, significantly improving sexual function and satisfaction, compared with men remaining on a comparable dose of AndroGel. In addition, a significantly higher portion of subjects receiving Testim did not require dose escalation to achieve results at the end of the study period, compared with AndroGel. The study enrolled a total of 151 hypogonadal men who were refractory to or insufficiently served by AndroGel therapy; these subjects were randomized to receive either continued treatments with AndroGel or Testim once daily for 4 weeks.
July 12, 2004
Zonagen announced positive preliminary results of their phase I/II study of Androxal (clomiphene), an estrogen antagonist, for the treatment of testosterone deficiency in men. Results indicated that the drug was safe and well tolerated, and produced significant increases in testosterone levels over placebo. The trial randomized a total of 70 hypogonadal men into one of 6 treatment arms: one of three doses of oral Androxal, one of two doses of topic Androgel (a currently approved topical gel for testosterone deficiency), or placebo. All subjects received daily dosing for two weeks to analyze safety and tolerability, and half of the subjects in each trial arm were examined on days 1 and 14 for pharmacokinetics and efficacy in increasing testosterone levels. Androxal was found to be comparable to placebo for all adverse events, and it produced significant, dose dependent increases in testosterone levels during a 7-10 day observation period following administration at all dose levels. Zonagen indicated that they would announce final results, including comparative data for Androxal vs. Androgel, later this year.
July 7, 2003
Neurocrine Biosciences reported positive results from a phase I trial investigating NBI-42902, a GnRH receptor antagonist for the treatment of hormone dependent diseases. Results demonstrated that NBI-42902 was absorbed rapidly after oral administration and was found to be safe and well tolerated. Gonadal suppression was achieved and resulted in suppression of estrogen to anticipated therapeutic levels. The randomized, double blind, placebo-controlled, parallel group study enrolled 18 healthy pre-menopausal women. Subjects were assigned to three groups, NBI-42902 75 mg once a day, NBI-42902 37.5 mg twice a day or placebo. Data indicated suppression of luteinizing hormone and follicle-stimulating hormones as expected based on data from previous studies.