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Home » Santa Clarita News » Health And Beauty » MannKind Corp. Announced FDA Approval Of Diabetes Treatment
MannKind Corp. Announced FDA Approval Of Diabetes Treatment

MannKind Corp. Announced FDA Approval Of Diabetes Treatment

The MannKind Corp. announced that it has receive the FDA approval for its candidate diabetes treatment, Afrezza. The announcement came after the close of trading Friday.

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The third time was the charm for the Valencia-based company and its revolutionary whistle-sized insulin inhaler, which acts more rapidly than Eli Lilly’s or Novo Nordisk’s injectable insulins and reduces or eliminates the need for needles completely, depending on the patient’s specific type of diabetes.

The FDA had rejected MannKind’s application for approval twice before, saying more clinical trials were needed. The company completed them.

In Friday’s statement, MannKind, which sought approval for Afrezza as a treatment for both type-1 and type-2 diabetes, said the FDA approved the drug “to improve glycemic control in adult patients with diabetes mellitus.” The approval came with the restriction that for patients with type-1 diabetes mellitus, Afrezza must be used “in combination with a long-acting insulin.” Also, it is “not recommended for the treatment of diabetic ketoacidosis” or “patients who smoke.”

Wall Street was expecting approval but was nervous about potential restrictions. Following approval, much of the investor commentary focused on the requirement of a warning label on the box, cautioning patients with chronic lung disease that they could be risk for acute bronchospam.

Whether Friday’s decision was quite the level of full-blown approval the company was seeking is unclear, but it’s a first for billionaire Alfred Mann’s 11-year-old pharmaceutical firm, which has been in the research and development phase and hasn’t yet had a salable product since the company organized as a merger of three other Al Mann companies in 2003. It operates out of the Mann Biomedical Park in Rye Canyon in Valencia and operates a facility in Danbury, Conn.

Now, MannKind will be on the lookout for a marketing partner.

Related Story: FCDH To Close Monday After 21 Years Of Operation In SCV


MannKind Corporation today announced that the U.S. Food & Drug Administration (FDA) has approved AFREZZA(R) (insulin human) Inhalation Powder to improve glycemic control in adult patients with diabetes mellitus.

“Approval of AFREZZA is an important milestone for MannKind, as today’s FDA action validates the years of clinical research and commitment that powered the development of this unique therapy,” said Alfred Mann, Chief Executive Officer, MannKind Corporation. “We are excited for patients, as we believe that AFREZZA’s distinct profile and non-injectable administration will address many of their unmet needs for mealtime insulin therapy, and has the potential to change the way that diabetes is treated. We thank the more than 6,500 adult patients and healthy volunteers who participated in the AFREZZA clinical program.”

Currently, diabetes mellitus affects 29.1 million people in the United States, according to the Centers for Disease Control and Prevention. Diabetes mellitus is characterized by the body’s inability to regulate levels of blood glucose properly. Insulin, a hormone produced by the pancreas, normally regulates the body’s glucose levels, but in people with diabetes mellitus insufficient levels of insulin are produced or the body fails to respond adequately to the insulin it produces. In patients with diabetes, current injected insulins are absorbed into the bloodstream slower than the body’s own insulin would be released if the pancreas was healthy.

AFREZZA(R) (uh-FREZZ-uh) is a novel, rapid-acting inhaled insulin therapy indicated to improve glycemic control in adult patients with diabetes mellitus. The product consists of AFREZZA Inhalation Powder delivered using a small, discreet and easy-to-use inhaler. Administered at the start of a meal, AFREZZA dissolves rapidly upon inhalation to the deep lung and delivers insulin quickly to the bloodstream. Peak insulin levels are achieved within 12 to 15 minutes of administration, and decline to baseline by approximately 180 minutes.

“The FDA approval of AFREZZA provides healthcare professionals with an important new safe and effective treatment option for patients with diabetes,” said Janet McGill, M.D., Professor of Medicine at Washington University School of Medicine. “We have seen in clinical studies that the combination of rapid action, injection-free delivery and ease of use makes AFREZZA a welcome alternative for many patients who require insulin.”

LIMITATIONS OF USE: AFREZZA must be used in combination with a long-acting insulin in patients with type 1 diabetes mellitus. AFREZZA is not recommended for the treatment of diabetic ketoacidosis and is not recommended for patients who smoke.

Full US Prescribing Information, including BOXED WARNING, Medication Guide and Instructions for Use will soon be available at Prior to the label being posted online, a copy of the label may be requested from the MannKind Media contacts listed at the end of this document.

AFREZZA has been approved with a Risk Evaluation and Mitigation Strategy (REMS) required by the FDA to ensure that the benefits of AFREZZA outweigh the potential risk of acute bronchospasm in patients with chronic lung disease.

Important Safety Information about AFREZZA (insulin human Inhalation Powder)
The following information is taken from the highlights section of the US Prescribing Information. Please see full Prescribing Information including boxed warning.


Acute bronchospasm has been observed in patients with asthma and COPD using AFREZZA. AFREZZA is contraindicated in patients with chronic lung disease such as asthma or COPD.
Before initiating AFREZZA, perform a detailed medical history, physical examination and spirometry (FEV1) to identify potential lung disease in all patients.

AFREZZA is contraindicated during episodes of hypoglycemia, in patients with chronic lung disease such as asthma or chronic obstructive pulmonary disease (COPD), or in patients with a hypersensitivity to regular human insulin or any of the AFREZZA excipients.

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Acute Bronchospasm: Acute bronchospasm has been observed in patients with asthma and COPD. Before initiating, perform spirometry (FEV1) in all patients. Do not use in patients with chronic lung disease.

Change in Insulin Regimen: Carry out under close medical supervision and increase frequency of blood glucose monitoring.

Hypoglycemia: May be life-threatening. Increase frequency of glucose monitoring with changes to; insulin dosage, co-administered glucose lowering medications, meal pattern, physical activity; and in patients with renal or hepatic impairment and hypoglycemia unawareness.

Decline in Pulmonary Function: Assess pulmonary function (e.g., spirometry) before initiating, after 6 months of therapy, and annually, even in the absence of pulmonary symptoms.

Lung Cancer: AFREZZA should not be used in patients with active lung cancer. In patients with a history of lung cancer or at risk for lung cancer, the benefit of AFREZZA use should outweigh this potential risk.

Diabetic Ketoacidosis: More patients using AFREZZA experienced diabetic ketoacidosis in clinical trials. In patients at risk for DKA, monitor and change to alternate route of insulin delivery, if indicated.

Hypersensitivity Reactions: May be life-threatening. Discontinue AFREZZA, monitor and treat if indicated.

Hypokalemia: May be life-threatening. Monitor Potassium levels in patients at risk of hypokalemia and treat if indicated.

Fluid Retention and Heart Failure with Concomitant Use of Thiazolidinediones (TZDs): Observe for signs and symptoms of heart failure; consider dosage reduction or discontinuation if heart failure occurs.


The most common adverse reactions associated with AFREZZA (2% or greater incidence) are hypoglycemia, cough, and throat pain or irritation.

About MannKind Corporation

MannKind Corporation (MNKD) focuses on the discovery, development and commercialization of therapeutic products for patients with diseases such as diabetes. MannKind maintains a website at to which MannKind regularly posts copies of its press releases as well as additional information about MannKind. Interested persons can subscribe on the MannKind website to e-mail alerts that are sent automatically when MannKind issues press releases, files its reports with the Securities and Exchange Commission or posts certain other information to the website.

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MannKind Corp. Announced FDA Approval Of Diabetes Treatment

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