Monoferric moments

Hear from healthcare providers treating IDA on why they choose Monoferric for their patients

Jonathan Ogden, PharmD, discusses the benefits of Monoferric

Hi, I'm John Ogden, PharmD and welcome to Monoferric Moments.

For the last 14 years, I've been the director of pharmacy operations at a large oncology practice located in the Southern United States.

We primarily treat adult oncology and hematology patients, as well as treating patients with iron deficiency anemias due to several different etiologies, which include heavy menstrual bleeding, inflammatory bowel disease, post-bariatric surgery, and cancer induced anemia.

In my experience, treatment options for iron deficiency anemia have evolved so much in recent years.

There are so many options now and no parity among dosing, so really we have to decide what's best for each individual patient.

In my experience, one of the largest bears to maintaining a regimen designed to treat iron deficiency anemia is the actual logistics of getting the patient to the clinic.

If they don't get in to get their entire dose, they run the risk of having worsening symptoms of their iron deficiency anemia.

Additional operational challenges that we have to consider with the treatment of iron deficiency anemia have to do with possibly scheduling a patient anywhere from two to five times to receive their full dose of IV iron.

This can lead to busier clinic days, more stress for the patient, and more stress to our staff.

Monoferric is actually the preferred IV iron product in our clinic and has been for the last couple of years.

Our physicians like the idea that a patient can receive their entire iron dose in a single dose, and we haven't noticed a significant difference in adverse events compared to other IV iron products.

Some of the benefits of a single dose option of Monoferric include the fact that the patient only has to come to the clinic one time to get their full dose of IV iron.

This also reduces the amount of patients that we have to schedule in our clinic leading to less workload and less stress on our nurses.

I certainly consider hypophosphatemia incident rates when determining high dose IV iron product in my clinic.

Knowing that Monoferric has head-to-head data measuring hypophosphatemia published in JAMA, I feel more comfortable recommending it, especially in high risk populations.

In my experience, the Monoferric Patient Solutions program has been excellent in helping improve the patient journey.

From a front office perspective, the quick response times and customized support you receive from Monoferric are a huge help.

I love to see all our nurses educated on the intricacies of treatment, and Monoferric has a comprehensive nurse educator program.

The tools and flow sheets they use are easy to follow and ensure our nurses are prepared to administer Monoferric.

Recently, I had to have a vial replaced for a patient, and I was impressed with the speed and ease of the process.

As a director of pharmacy operations, I choose Monoferric at my practice because it gives our staff and our patients a one dose option to address iron deficiency anemia.

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Introducing Dr Huzefa Bahrain

I’m Dr Huzefa Bahrain, welcome to Monoferric Moments.

I practice hematology and oncology in Baltimore. We operate an erythropoiesis center where we treat a wide variety of patients with various iron deficiency anemia etiologies. They can range from bariatric surgery patients to heart failure, to pregnancy.

Monoferric is an intravenous iron replacement therapy that can be given in just 1 single dose, delivering 1000 milligrams.

In my experience, we find that for most patients, just 1 dose of 1000 milligrams of Monoferric is sufficient to replace iron stores. If iron deficiency anemia reoccurs, a repeat dose would be necessary.

I use Monoferric in my practice because of its overall combination of 1-dose administration, efficacy, tolerability, and patient support services.

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Dr Bahrain discusses efficacy and safety

I’m Dr Huzefa Bahrain, welcome to Monoferric Moments.

In my experience, we find that for most patients, just 1 dose of 1000 milligrams of Monoferric is sufficient to replenish iron stores.

Looking at all the intravenous iron infusions we’ve administered through clinical trials and commercial patients, Monoferric is observed as having a solid safety profile that is comparable to iron sucrose and is generally well tolerated by the vast majority of patients.

Monoferric has been evaluated in two clinical trials with a total of 3050 patients.

When looking at safety, there was no significant differences in adjudicated serious or severe hypersensitivity reactions between Monoferric and iron sucrose.

Only 0.3 percent of patients reported adjudicated serious or severe hypersensitivity reactions.

Monoferric was also evaluated in the PHOSPHARE study, which was two identical safety trials that were pooled to compare the incidence of hypophosphatemia with Monoferric vs ferric carboxymaltose.

Monoferric demonstrated significantly fewer incidences of hypophosphatemia than ferric carboxymaltose from baseline to day 35.

In the PHOSPHARE study pooled results, only 8.0% of patients treated with Monoferric versus 74.4% of those treated with ferric carboxymaltose were noted to have hypophosphatemia.

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Dr Bahrain discusses the Monoferric Patient Solutions® Program

The The Monoferric Patient Solutions® Program has been helpful to those who have trouble accessing intravenous iron. The program is well coordinated and supportive to the patients and their needs.

There is also the availability of Nurse Educators for infusion staff.

Learn about access and support

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IDA=iron deficiency anemia.

IMPORTANT SAFETY INFORMATION

Monoferric is contraindicated in patients with a history of serious hypersensitivity to Monoferric or any of its components. Reactions have included shock, clinically significant hypotension, loss of consciousness, and/or collapse.

INDICATIONS

Monoferric is indicated for the treatment of iron deficiency anemia (IDA) in adult patients:

  • who have intolerance to oral iron or have had unsatisfactory response to oral iron
  • who have non-hemodialysis dependent chronic kidney disease (NDD-CKD)

IMPORTANT SAFETY INFORMATION

CONTRAINDICATIONS

Monoferric is contraindicated in patients with a history of serious hypersensitivity to Monoferric or any of its components. Reactions have included shock, clinically significant hypotension, loss of consciousness, and/or collapse.

WARNINGS AND PRECAUTIONS

Hypersensitivity Reactions

Serious hypersensitivity reactions, including anaphylactic-type reactions, some of which have been life-threatening and fatal, have been reported in patients receiving Monoferric. Patients may present with shock, clinically significant hypotension, loss of consciousness, and/or collapse. Monitor patients for signs and symptoms of hypersensitivity during and after Monoferric administration for at least 30 minutes and until clinically stable following completion of the infusion. Only administer Monoferric when personnel and therapies are immediately available for the treatment of serious hypersensitivity reactions. Monoferric is contraindicated in patients with prior serious hypersensitivity reactions to Monoferric or any of its components. In clinical trials in patients with IDA and CKD, serious or severe hypersensitivity were reported in 0.3% (6/2008) of the Monoferric treated subjects. These included 3 events of hypersensitivity in 3 patients; 2 events of infusion-related reactions in 2 patients and 1 event of asthma in one patient.

Iron Overload

Excessive therapy with parenteral iron can lead to excess iron storage and possibly iatrogenic hemosiderosis or hemochromatosis. Monitor the hematologic response (hemoglobin and hematocrit) and iron parameters (serum ferritin and transferrin saturation) during parenteral iron therapy. Do not administer Monoferric to patients with iron overload.

ADVERSE REACTIONS

Adverse reactions were reported in 8.6% (172/2008) of patients treated with Monoferric. Adverse reactions related to treatment and reported by ≥1% of the treated patients were nausea (1.2%) and rash (1%). Adjudicated serious or severe hypersensitivity reactions were reported in 6/2008 (0.3%) patients in the Monoferric group. Hypophosphatemia (serum phosphate <2.0 mg/dL) was reported in 3.5% of Monoferric-treated patients in Trials 1 & 2.

To report adverse events, please contact Pharmacosmos at 1-888-828-0655. You may also contact the FDA at www.fda.gov/medwatch or 1-800-FDA-1088.

Please see Full Prescribing Information.