Advanced Cell Technology Inc., of Santa Monica, Calif., said it has treated 13 patients thus far in its three ongoing trials for dry age-related macular degeneration and Stargardt's disease using human embryonic stem cell-derived retinal pigment epithelial cells. The first two trials began in July 2011. The three clinical trials involve four of the top-ranked eye hospitals in the U.S., and two of the leading eye hospitals in the UK. Across the various clinical trial sites, with regular patient

Boehringer Ingelheim Pharmaceuticals Inc., of Ridgefield, Conn., part of Boehringer Ingelheim GmbH, disclosed interim results from the RELY-ABLE trial, a long-term extension of the RE-LY study. During more than two years of randomized follow-up, key safety outcomes such as major bleeding, total bleeding and life-threatening bleeding were similar to the results of the dabigatran 110-mg and 150-mg arms of the pivotal RE-LY trial that evaluated Pradaxa (dabigatran etexilate mesylate) capsules in

Amgen Inc., of Thousand Oaks, Calif., reported results from the LAPLACE-TIMI 57 and MENDEL Phase II studies testing AMG 145 in hypercholesterolemic patients with or without statins, respectively, showing that treatment with the PCSK9-directed antibody resulted in a statistically significant reduction in low-density lipoprotein cholesterol (LDL-C). All six dose regimens of AMG 145 significantly decreased LDL-C, measured by preparative ultracentrifugation, from baseline vs. placebo at week 12 in

Array BioPharma Inc., of Boulder, Colo., reviewed the abstracts released ahead of the American Society of Hematology meeting next month, showing that ARRY-520, a dual p38/Tie2 inhibitor, plus low-dose dexamethasone produced a 22 percent overall response rate in patients with triple-refractory multiple myeloma who have had a median number of 10 prior treatment regimens. In a related abstract assessing the same group of patients, the company said that prospective screening for the acute phase

Taiho Pharmaceutical Co. Ltd., of Tokyo, presented early stage data for multiple oncology compounds at the EORTC-NCI-AACR Symposium on Molecular Targets and Cancer Therapeutics in Dublin, Irealnd, including Phase II results showing that TAS-102 produced an improvement in overall survival in patients with metastatic colorectal cancer. Additional presentations focused on TAS-114, a dUTPase dual and DPD dual inhibitor, and TAS-115, a dual inhibitor of hepatocyte and vascular endothelial growth

Aegerion Pharmaceuticals Inc., of Cambridge, Mass., said results were published in The Lancet from the firm's 78-week pivotal Phase III study of lomitapide in adult patients with homozygous familial hypercholesterolemia. The compound was recommended for approval by an FDA advisory panel last month. (See BioWorld Today, Oct. 18, 2002.) Aerie Pharmaceuticals Inc., of Bedminster, N.J., disclosed positive top-line results from its Phase IIa study evaluating AR-13324 for the treatment of glaucoma

Aegerion Pharmaceuticals Inc., of Cambridge, Mass., said results were published in The Lancet from the firm's 78-week pivotal Phase III study of lomitapide in adult patients with homozygous familial hypercholesterolemia. The compound was recommended for approval by an FDA advisory panel last month. (See BioWorld Today, Oct. 18, 2002.) Aerie Pharmaceuticals Inc., of Bedminster, N.J., disclosed positive top-line results from its Phase IIa study evaluating AR-13324 for the treatment of glaucoma

Advaxis Inc., of Princeton, N.J., presented updated data at the Society for Immunotherapy of Cancer meeting in North Bethesda, Md., from its ongoing 110-patient Phase II trial testing ADXS-HPV vs. ADXS-HPV plus cisplatin in India in women with recurrent/refractory cervical cancer who have failed previous cytotoxic therapy. As of Oct. 22, landmark survival at six months, nine months, 12 months and 18 months was 65 percent, 44 percent, 33 percent and 17 percent, respectively, with no apparent

Asahi Kasei Pharma America Corp., of Waltham, Mass., said it started an 800-patient Phase III trial of ART-123 (recombinant human thrombomodulin, sold as Recomodulin in Japan) in severe sepsis patients with coagulopathy. The study is designed to measure 28-day all-cause mortality as its primary efficacy endpoint; primary safety measures include serious adverse events, adverse events and major bleeding events. Secondary endpoints include all-cause mortality at three months and resolution of

AB Science SA, of Paris, reported Phase III results showing that masitinib in combination with Gemzar (gemcitabine, Eli Lilly and Co.) significantly extended overall survival in patients with pancreatic cancer by six months and 2.7 months in two independent patient populations, representing 65 percent and 45 percent of the overall population – namely, patients with a genetic biomarker indicative of aggressive disease progression. AB Science also said the European Medicines Agency accepted for

AstraZeneca plc, of London, said it started a Phase III study, dubbed FALCON, to compare fulvestrant to Arimidex (anastrozole) in hormone therapy-naïve postmenopausal patients with hormone receptor-positive locally advanced or metastatic breast cancer. The study is expected to involve 450 women and will evaluate the efficacy and tolerability of fulvestrant 500 mg compared to anastrozole 1 mg.

Biogen Idec Inc., of Weston, Mass., reported in its third-quarter earnings call that it will not proceed with a planned Phase IIa rheumatoid arthritis (RA) study of its Syk inhibitor partnered with Portola Pharmaceuticals Inc., of South San Francisco. Biogen said the compound did not meet the "stringent target product profile to be competitive in this specific market." The companies, which entered the potential $553.5 million Syk collaboration last year, will continue exploratory work in

Daiichi Sankyo Co. Ltd., of Tokyo, said it completed patient enrollment in the Hokusai-VTE Phase III study testing once-daily oral Factor Xa inhibitor edoxaban for the treatment and prevention of recurrence of venous thromboembolism in patients who have had an acute symptomatic deep vein thrombosis, pulmonary embolism or both.

Teva Pharmaceutical Industries Ltd., of Jerusalem, said its women's health subsidiary reported Phase III findings showing that Quartette (levonorgestrel/ethinyl estradiol tablets and ethinyl estradiol tablets), an extended-regimen oral contraceptive, showed the product is efficacious for the prevention of pregnancy and has a safety profile similar to those of other oral contraceptives. Data were presented at the American Society of Reproductive Medicine meeting in San Diego.

Astex Pharmaceuticals Inc., of Dublin, Calif., said it started an open-label Phase II trial testing Hsp90 inhibitor AT13387 in anaplastic lymphoma kinase-positive non-small-cell lung cancer (NSCLC) patients or other potentially Xalkori- (crizotinib, Pfizer Inc.) sensitive NSCLC patients who have been receiving Xalkori. The study will test AT13387 as both a single agent and in combination with Xalkori. The study will consist of three parts: The primary objective of Part A is to determine safety

Abbott, of Abbott Park, Ill., said results from a post-hoc subanalysis of the 52-week Humira (adalimumab) ULTRA 2 study showed clinically meaningful rates of mucosal healing at week 52 in patients with moderately to severely active ulcerative colitis who failed, were intolerant or had contraindications to certain other medications and achieved a response to Humira induction therapy at eight weeks. Of the 494 patients included in the analysis and who responded at eight weeks, significantly more

Agenus Inc., of Lexington, Mass., said it started a Phase II study of HerpV, a recombinant off-the-shelf therapeutic vaccine candidate, containing the company's QS-21 Stimulon adjuvant, for treating genital herpes in herpes simplex virus 2-positive subjects. The study will enroll 75 patients who have a history of frequent disease recurrences and will test the efficacy of the vaccine as measured by effect on genital viral shedding. Celgene Corp., of Summit, N.J., said its Celgene International

Abbott, of Abbott Park, Ill., said results from three-year long-term data from an ongoing extension study of the Humira (adalimumab) ULTRA 1 and ULTRA 2 studies in ulcerative colitis showed a reduction in observed mean Partial Mayo score from 5.9 at the time of first Humira dose to 1.4 at week 172. A 55.3 percent remission rate, per Partial May score, at week 60 of the extension study also was seen. Data were presented at the American College of Gastroenterology meeting in Las Vegas. Eli

Histogen Inc., of San Diego, said preliminary data from an ongoing Phase I/II study showed that its Hair Stimulating Complex (HSC) produced statistically significant improvement across all targeted hair growth parameters, with an 86 percent responder rate. The study tested HSC in 56 men with androgenetic alopecia and also was well tolerated, with no study-related adverse events reported. Data were presented at the International Society of Hair Restoration Surgery meeting in the Bahamas. Ipsen