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Saturday, July 6, 2019

Diabetes Medications Increase Fracture Risk

Insulinthiazolidinedione, and sulphonylureasmay be associated with a greater risk of fracture, a new study has found.
Patients with diabetes mellitus (DM) have increased morbidity and mortality rates, according to the study authors, and some research has suggested they have a greater likelihood of fracture. “While the biological mechanisms underlying the positive association between DM and the risk of fracture remain largely obscure, a higher propensity of falling, impairment of bone quality, and direct or indirect treatment effects of glucose‐lowering medications on bone have been suggested to explain the elevated risk of fracture among DM patients,” they reported in their meta-analysis, published in Obesity Reviews. And while past studies have found a link between thiazolidinedione and fracture, data are limited on the association between thiazolidinedione as well as insulin, sulphonylureas, and metformin and fracture.
The researchers queried PubMed and Web of Science databases for relevant observational studies from inception through February using a combination of these search terms: (diabetes OR insulin OR glargine OR lispro OR biguanidine OR metformin OR thiazolidinediones OR pioglitazone OR rosiglitazone OR sulfonylureas OR sulphonylureas OR acetohexamide OR carbutamide OR chlorpropamide OR glycyclamide OR metahexamide OR tolazamide OR tolbutamide OR glibenclamide OR glibornuride OR gliclazide OR glipizide OR gliquidone OR glisoxepide OR glyclopyramide OR glimepiride) and fracture.

Metformin May Be Safest Bet for Low Fracture Risk

The final analysis included 33 studies, of which 26 were cohort and seven were case-control studies. An estimated 345,133 fractures were reported in about 6,847,158 patients. Studies reported on the use of metformin (n = 12), insulin (n = 23), sulphonylureas (n = 10), and thiazolidinediones (n = 14). Fracture risk was increased among patients using insulin (relative risk [RR] 1.49, 95% confidence interval [CI] 1.29-1.73), sulphonylureas (RR 1.30, 95% CI 1.18-1.43), and thiazolidinediones (RR 1.24, 95% CI 1.13-1.35), while fracture risk was decreased among patients using metformin (RR 0.86, 95% CI 0.75-0.99).
When assessing fracture risk associated with different types of thiazolidinediones, RRs were similar between pioglitazone (1.38, 95% CI 1.23-1.54) and rosiglitazone (1.34, 95% CI 1.14-1.58) use.
“The positive association between insulin or thiazolidinedione use and the risk of fracture was attenuated to non‐significant in the studies that adjusted for certain variables (falls or previous fracture for insulin and osteoporosis/osteoporosis medications, steroid medications, or classic glucose‐lowering medications for thiazolidinediones); this result was possibly driven by the contradictory studies reporting a significant reduction in risk with the use of insulin and thiazolidinediones, as the associations became significant after exclusion of these studies (data not shown),” the researchers further observed. “Furthermore, the association between thiazolidinedione use and the risk of hip fracture became significant (RR 1.21, 95% CI 1.03, 1.43) after exclusion of a contradictory study.”
The study authors concluded that thiazolidinedione use should be discouraged among patients at a high risk of fracture. Insulin and sulphonylurea use may increase fracture risk as well, “which is most likely attributed to an increased risk of hypoglycaemia‐induced falls,” they said. Therefore, when prescribing insulin and sulphonylureas, a patient’s risk of hypoglycemia should be considered. Metformin appeared to have a good safety profile in terms of fracture risk. Still, the researchers called for randomized controlled trials to determine whether certain medications do increase fracture risk or if other confounding factors are at play.

Mixed shelf filing roundup – healthcare

The following healthcare companies have filed prospectuses for mixed shelf offerings:
Translate Bio (NASDAQ:TBIO): $250M.
Cellular Biomedicine Group (NASDAQ:CBMG): $200M.
Iterum Therapeutics (NASDAQ:ITRM): $150M.

Glucose Biosensor Systems (Greater China) Holdings readies IPO

The New York City-based medical tech company plans to launch its Saliva Glucose Biosensor test in Mainland China, Hong Kong, Vietnam and Bangladesh, followed by tests for prostate specific antigen, peanut allergen and luteinizing hormone.
The Saliva Glucose Biosensor test, a non-invasive method of measuring glucose, is based on an electrochemical reaction that produces an electrical signal that is directly proportional to the amount of glucose in the saliva. A smart phone app converts the signal into a real-time glucose reading that can be stored in the company’s cloud-based digital information system.
Financials (nine-month period ending March 31, 2019): Sales: $114.0K; Net Loss: ($4.2M); Cash Consumption: ($3.1M).

Rapt Therapeutics files for IPO

Rapt Therapeutics (OTC:RAPT) has filed a preliminary prospectus for an $86M IPO.
The South San Francisco-based biopharma firm develops small molecule therapies for cancer and inflammatory disorders that it says modulate the critical immune responses underlying the diseases.
Lead oncology candidate is FLX475, a CCR4 antagonist that blocks the migration of immunosuppressive regulatory T cells into tumors. Proof-of-concept data should be available in H1 2020.
Lead inflammation candidate is RPT193, also a CCR4 antagonist, that blocks the recruitment of inflammatory immune cells called type 2 T helper cells that play a key role in allergic inflammatory diseases. A Phase 1 study in atopic dermatitis should launch in H2.
2019 Financials (Q1): Operating Expenses: $9.5M (+14.1%); Net Loss: ($9.2M) (-11.6%); Cash Burn: ($8.6M) (-13.4%).

Sangamo, Pfizer Update Phase 1/2 Results for Hemophilia A Gene Therapy

  • The first two patients treated at the 3e13 vg/kg dose level rapidly achieved normal, sustained Factor VIII (FVIII) levels with no reported bleeding events and no factor usage for as long as 24 weeks of follow-up
  • The two patients more recently treated at the 3e13 vg/kg dose level demonstrated FVIII activity kinetics that appear consistent with the first two patients in this dose cohort at similar early time points
  • SB-525 showed dose-dependent increases in FVIII activity levels across all dose cohorts evaluated
  • FDA recently granted regenerative medicine advanced therapy (RMAT) designation for SB-525 gene therapy to treat severe hemophilia A

uniQure Has Follow-Up Data from Phase 2b Hemophilia B Study

~ FIX Activity Up to 54% of Normal, with Mean of 45% of Normal, at 36 WeeksAfter Administration of AMT-061 in Phase IIb Study ~
~ Clinical Benefit and Tolerability of AMT-060 Maintained in All Patients Through up to 3.5 Years of Follow-up ~
uniQure N.V. (NASDAQ: QURE), a leading gene therapy company advancing transformative therapies for patients with severe medical needs, today announced updated clinical data on the three patients treated in the Company’s ongoing Phase IIb study of AMT-061, an investigational AAV5-based gene therapy containing a patent-protected FIX-Padua variant for the treatment of patients with severe and moderately severe hemophilia B. In addition, the Company presented up to 3.5 years of follow-up data on the 10 patients in the Phase I/II trial of AMT-060, its first-generation gene therapy for the treatment of hemophilia B. These clinical data were presented on Saturday, July 6 in oral presentations at the 27th Congress of the International Society on Thrombosis and Haemostasis (ISTH), taking place in Melbourne, Australia.
Featured in an oral presentation at ISTH, the 36 weeks of follow-up data show that all three patients have sustained increases in FIX levels after the one-time administration of AMT-061, with two of the three patients maintaining FIX activity in the normal range. Mean FIX activity for the three patients at 36 weeks after administration was 45% of normal, with the first patient achieving FIX activity of 54% of normal, the second patient achieving FIX activity of 30% of normal and the third patient achieving FIX activity of 51% of normal. The second and third patients had previously screen-failed and were excluded from another gene therapy study due to pre-existing neutralizing antibodies to a different AAV vector. Reported FIX activity was measured using an activated partial thromboplastin time (aPTT) assay performed at a central laboratory.
No patient in the study has experienced a material loss of FIX activity, reported any bleeding events or required any infusions of FIX replacement therapy for bleeds. One patient underwent hip surgery due to a pre-existing condition and was treated perioperatively with short-acting factor replacement. This was reported by the investigator as a serious adverse event unrelated to AMT-061.
“These updated data continue to show that a single administration of AMT-061 is well-tolerated and has the potential to increase FIX activity into the normal range for people living with hemophilia B,” stated Matt Kapusta, chief executive officer of uniQure. “We continue to be very pleased with these results, which as of this data report show durable increases in FIX activity with no bleeds and no requirement for infusions of FIX replacement therapy or immunosuppression. We believe AMT-061 has the potential to be a first- and best-in-class gene therapy for patients with hemophilia B, and we remain focused on our goal of completing enrollment in our ongoing HOPE-B pivotal trial by the end of this year.”

Array Interim Results of Colorectal Cancer Trial at ESMO Meet

BRAFTOVI combinations showed statistically significant improvement in OS and ORR versus control – – Data supports potential to be the first chemotherapy-free, targeted regimen for BRAF-mutant mCRC patients – – Results were presented in an oral presentation today, July 6, 2019

Array BioPharma Inc. (Nasdaq: ARRY) today announced the presentation of results from the Phase 3 BEACON CRC trial evaluating the combination of BRAFTOVI® (encorafenib), a BRAF inhibitor, MEKTOVI® (binimetinib), a MEK inhibitor, and ERBITUX® (cetuximab), an anti-EGFR antibody (BRAFTOVI Triplet), in patients with advanced BRAFV600E-mutant metastatic colorectal cancer (mCRC), following one or two lines of therapy. Data presented included primary and secondary endpoints, waterfall plots describing tumor reduction, subgroup analyses, and exploratory analyses comparing overall survival (OS) of the BRAFTOVI Triplet and BRAFTOVI Doublet (BRAFTOVI and cetuximab) in a subset of patients with mature follow-up, including the first 331 randomized patients, as well as safety and tolerability.
Results showed that BRAF-mutant mCRC patients treated with the BRAFTOVI Triplet combination demonstrated a statistically significant improvement in OS (9.0 months vs. 5.4 months, [HR 0.52, (95% CI 0.39-0.70), p<0.0001]) and objective response rate (ORR) (26.1% vs. 1.9%, p<0.0001, as assessed by Blinded Independent Central Review (BICR)) compared to cetuximab plus irinotecan-containing regimens (Control). Median progression-free survival (mPFS) for patients treated with the BRAFTOVI Triplet was 4.3 months [HR 0.38, (95% CI 0.29, 0.49), p<0.0001] compared to 1.5 months observed with the Control arm.
These data were presented in an oral presentation on Saturday, July 6, at the ESMO 21st World Congress on Gastrointestinal Cancer in Barcelona, Spain.