Gammaplex label

Gammaplex

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Side Effects & Adverse Reactions

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FDA Safety Alerts

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Manufacturer Warnings

There is currently no manufacturer warning information available for this drug.

FDA Labeling Changes

There are currently no FDA labeling changes available for this drug.

Uses

1.1 Primary Humoral Immunodeficiency (PI)

Gammaplex is an Immune Globulin Intravenous (Human), 5% Liquid indicated for replacement therapy in adults with primary humoral immunodeficiency (PI). This includes, but is not limited to, the humoral immune defect in common variable immunodeficiency, X-linked agammaglobulinemia, congenital agammaglobulinemia, Wiskott-Aldrich syndrome, and severe combined immunodeficiencies.

1.2 Chronic Immune Thrombocytopenic Purpura (ITP)

Gammaplex is indicated for the treatment of adults with chronic immune thrombocytopenic purpura (ITP) to raise platelet counts.

History

There is currently no drug history available for this drug.

Other Information

Gammaplex is a ready to use sterile solution of polyclonal human Immunoglobulin G for intravenous administration that contains sorbitol, glycine and polysorbate 80 as stabilizers. Specifically, Gammaplex contains approximately 5 g normal human immunoglobulin and 5 g D-sorbitol in 100 mL of buffer solution containing: 0.6 g glycine, 0.2 g sodium acetate, 0.3 g sodium chloride and ~5 mg polysorbate 80. Immunoglobulin G purity is > 95%, the pH is in the range of 4.8 to 5.1, and osmolality is not less than 240 mOsmol/kg (typically 420 to 500 mOsmol/kg). The distribution of the four IgG subclasses is approximately 64% IgG1, 30% IgG2, 5% IgG3, and 1% IgG4. The content of IgA is lower than 10 μg/mL. The anti-D and anti-A/anti-B hemagglutinin content of the drug product is strictly controlled to specification. Gammaplex contains no reducing carbohydrate stabilizers (e.g. sucrose, maltose) and no preservative.

Gammaplex is prepared from large pools of human plasma by a combination of cold ethanol fractionation and ion exchange chromatography. Fab functions tested include antigen binding activity, and Fc functions tested include complement activation and rubella antibody-mediated hemolysis.

Gammaplex is manufactured from plasma, obtained from healthy US donors, who have passed viral screening tests. All donors are subjected to medical examinations, laboratory tests, and a review of their medical history before being allowed to donate blood or plasma.

All plasma donations are screened for antibody to HIV-1/2 and HCV, and hepatitis B surface antigen (HBsAg). Additional testing of donations is carried out in plasma mini-pools (512 donations per pool) that undergo nucleic acid amplification testing (NAT) for HIV, hepatitis B virus (HBV), HCV, hepatitis A virus (HAV) and Parvovirus B19.

Further testing is carried out on the manufacturing pools for HBsAg, and antibody to HIV-1/2; HCV and Parvovirus B19 are also tested by NAT, with the limit for B19 set to not exceed 104 IU B19 DNA per mL plasma.

There are three processing steps specifically designed to remove or inactivate viruses:

1) Solvent/Detergent treatment is targeted to enveloped viruses;

2) A virus filtration step designed to remove small viruses including non-enveloped viruses, on a size exclusion basis; and

3) The terminal low pH incubation step is identified as contributing to the overall viral clearance capacity for enveloped and non-enveloped viruses.

The capacity of the manufacturing process to remove and/or inactivate enveloped and non-enveloped viruses has been validated by laboratory spiking studies on a scaled down process model. Overall virus reduction was calculated only from steps that were mechanistically independent from each other.

In addition, each step was validated to provide robust virus reduction. The table below presents the contribution of each process step to virus reduction and the overall process reduction.

Table 4: Viral Reduction by Process Step
Virus Type
(Envelope/ Genome)
Size
(nm)
Process Log10 Reduction of Virus (LRV) over manufacturing step
Solvent Detergent 20 nm filtration Terminal low pH/elevated temperature incubation Total LRV
HIV: Human immunodeficiency virus
SIN: Sindbis virus, model for hepatitis C virus (HCV)
WNV: West Nile Virus
BVDV: Bovine viral diarrhea virus, model for HCV
IBR: Infectious bovine rhinotracheitis, bovine herpesvirus model for enveloped DNA viruses including hepatitis B
HAV: Hepatitis A virus
EMC: Encephalomyocarditis, model for HAV
CPV: Canine parvovirus, model for human parvovirus B19
NA: Not applicable, solvent detergent step is limited to the inactivation of enveloped viruses
I: Inactivation by the product intermediate precluded the accurate estimation of the removal of these viruses by the filtration step
NT: Not tested
B19: Viral clearance of Human Parvovirus B19 was investigated experimentally at the 20 nm filtration step. The estimated Log reduction Factor obtained was 6.0
HIV Env/RNA 80-100 >6.8 I >6.1 >12.9
SIN Env/RNA 70 >6.7 6.2 >7.3 >20.2
WNV Env/RNA 50 >6.4 I NT >6.4
BVDV Env/RNA 40-60 >5.6 I >6.1 >11.7
IBR Env/DNA 200 >5.0 I >6.3 >11.3
HAV Non-Env/RNA 30 NA >4.8 1.1 >5.9
EMC Non-Env/RNA 30 NA >4.8 2.7 >7.5
CPV Non-Env/RNA 18-24 NA 3.2 1.4 4.6

Gammaplex Manufacturers

  • Bio Products Laboratory Limited
    Gammaplex | Mylan Pharmaceuticals Inc.
    No Recall

    Gammaplex | Mylan Pharmaceuticals Inc.

    Gammaplex | Mylan Pharmaceuticals Inc.
    2.1 Required Laboratory Testing Prior to Initiation and During Therapy

    Prior to initiating treatment with clozapine tablets, a baseline ANC must be obtained. The baseline ANC must be at least 1500/μL for the general population, and at least 1000/μL for patients with documented Benign Ethnic Neutropenia (BEN). To continue treatment, the ANC must be monitored regularly [see Warnings and Precautions (5.1)].

    2.2 Dosing Information

    The starting dose is 12.5 mg once daily or twice daily. The total daily dose can be increased in increments of 25 mg to 50 mg per day, if well-tolerated, to achieve a target dose of 300 mg to 450 mg per day (administered in divided doses) by the end of 2 weeks. Subsequently, the dose can be increased once weekly or twice weekly, in increments of up to 100 mg. The maximum dose is 900 mg per day. To minimize the risk of orthostatic hypotension, bradycardia, and syncope, it is necessary to use this low starting dose, gradual titration schedule, and divided dosages [see Warnings and Precautions (5.3)].

    Clozapine tablets can be taken with or without food [see Pharmacokinetics (12.3)].

    2.3 Maintenance Treatment

    Generally, patients responding to clozapine tablets should continue maintenance treatment on their effective dose beyond the acute episode.

    2.4 Discontinuation of Treatment

    Method of treatment discontinuation will vary depending on the patient’s last ANC:

    • See Tables 2 or 3 for appropriate ANC monitoring based on the level of neutropenia if abrupt treatment discontinuation is necessary because of moderate to severe neutropenia. • Reduce the dose gradually over a period of 1 to 2 weeks if termination of clozapine therapy is planned and there is no evidence of moderate to severe neutropenia. • For abrupt clozapine discontinuation for a reason unrelated to neutropenia, continuation of the existing ANC monitoring is recommended for general population patients until their ANC is ≥ 1500/μL and for BEN patients until their ANC is ≥ 1000/μL or above their baseline. • Additional ANC monitoring is required for any patient reporting onset of fever (temperature of 38.5°C or 101.3°F, or greater) during the 2 weeks after discontinuation [see Warnings and Precautions (5.1)]. • Monitor all patients carefully for the recurrence of psychotic symptoms and symptoms related to cholinergic rebound such as profuse sweating, headache, nausea, vomiting, and diarrhea. 2.5 Re-Initiation of Treatment

    When restarting clozapine tablets in patients who have discontinued clozapine tablets (i.e., 2 days or more since the last dose), re-initiate with 12.5 mg once daily or twice daily. This is necessary to minimize the risk of hypotension, bradycardia, and syncope [see Warnings and Precautions (5.3)]. If that dose is well-tolerated, the dose may be increased to the previously therapeutic dose more quickly than recommended for initial treatment.

    2.6 Dosage Adjustments with Concomitant Use of CYP1A2, CYP2D6, CYP3A4 Inhibitors or CYP1A2, CYP3A4 Inducers

    Dose adjustments may be necessary in patients with concomitant use of: strong CYP1A2 inhibitors (e.g., fluvoxamine, ciprofloxacin, or enoxacin); moderate or weak CYP1A2 inhibitors (e.g., oral contraceptives, or caffeine); CYP2D6 or CYP3A4 inhibitors (e.g., cimetidine, escitalopram, erythromycin, paroxetine, bupropion, fluoxetine, quinidine, duloxetine, terbinafine, or sertraline); CYP3A4 inducers (e.g., phenytoin, carbamazepine, St. John’s wort, and rifampin); or CYP1A2 inducers (e.g., tobacco smoking) (Table 1) [see Drug Interactions (7)].

    Table 1. Dose Adjustment in Patients Taking Concomitant Medications

    Co-medications

    Scenarios

    Initiating clozapine tablets while taking a co-medication

    Adding a co-medication while taking clozapine tablets

    Discontinuing a co-medication while continuing clozapine tablets

    Strong CYP1A2 Inhibitors

    Use one-third of the clozapine tablet dose.

    Increase clozapine tablet dose based on clinical response.

    Moderate or Weak

    CYP1A2 Inhibitors

    Monitor for adverse reactions. Consider reducing the clozapine tablet dose if necessary.

    Monitor for lack of effectiveness. Consider increasing clozapine tablet dose if necessary.

    CYP2D6 or CYP3A4 Inhibitors

    Strong CYP3A4 Inducers

    Concomitant use is not recommended. However, if the inducer is necessary, it may be necessary to increase the clozapine tablet dose. Monitor for decreased effectiveness.

    Reduce clozapine tablet dose based on clinical response.

    Moderate or weak CYP1A2 or CYP3A4 Inducers

    Monitor for decreased effectiveness. Consider increasing the clozapine tablet dose if necessary.

    Monitor for adverse reactions. Consider reducing the clozapine tablet dose if necessary.

    2.7 Renal or Hepatic Impairment or CYP2D6 Poor Metabolizers

    It may be necessary to reduce the clozapine tablet dose in patients with significant renal or hepatic impairment, or in CYP2D6 poor metabolizers [see Use in Specific Populations (8.6, 8.7)].

  • Bio Products Laboratory Limited
    Gammaplex | Bio Products Laboratory Limited
    No Recall

    Gammaplex | Bio Products Laboratory Limited

    Gammaplex | Bio Products Laboratory Limited

    For Intravenous Use Only

    Table 1: Recommended Dosage and Administration for Gammaplex Indication Dose Initial infusion rate Maintenance infusion rate (if tolerated) PI 300-800 mg/kg (6-16 mL/kg) every 3-4 weeks 0.5 mg/kg/min (0.01 mL/kg/min) for 15 min Increase gradually every 15 minutes to 4 mg/kg/min (0.08 mL/kg/min) ITP 1 g/kg (20 mL/kg) for 2 consecutive days 0.5 mg/kg/min (0.01 mL/kg/min) for 15 min Increase gradually every 15 minutes to 4 mg/kg/min (0.08 mL/kg/min) 2.1 Preparation and Handling Gammaplex is a clear or slightly opalescent, colorless solution. Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit. Do not use if the solution is cloudy or turbid, or if it contains particulate matter. Do not freeze, and do not use any solution that has been frozen. DO NOT SHAKE. Gammaplex should be at room temperature (up to 25°C [77°F]) at the time of administration. Do not use Gammaplex beyond the expiration date on the product label. The Gammaplex vial is for single use only. Due to the absence of anti-microbial preservatives, promptly administer Gammaplex after piercing the cap. Dispose of partially used or unused product. Infuse Gammaplex using a separate infusion line. Do not mix Gammaplex with other intravenous medications (including normal saline) or other IGIV products. An infusion pump may be used to control the rate of administration. If large doses of Gammaplex are to be administered, several vials may be pooled using aseptic technique. Begin infusion within 2 hours after pooling. 2.2 Recommended Dose

    Treatment of Primary Humoral Immunodeficiency

    As there are significant differences in the half-life of IgG among patients with PI, the frequency and amount of immunoglobulin therapy may vary from patient to patient. The proper amount can be determined by monitoring clinical response.

    The recommended dose of Gammaplex for patients with PI is 300 to 800 mg/kg (6 to 16 mL/kg), administered every 3 to 4 weeks. Adjust the dosage over time to achieve the desired serum trough levels and clinical response. If a patient misses a dose, administer the missed dose as soon as possible, and then resume scheduled treatments every 3 or 4 weeks, as applicable.

    Treatment of Chronic Immune Thrombocytopenic Purpura

    The recommended dose of Gammaplex for patients with ITP is 1 g/kg (20 mL/kg) on 2 consecutive days, providing a total dose of 2 g/kg. Carefully consider the relative risks and benefits before prescribing the high dose regimen (i.e. 1 g/kg/day for 2 days) in patients at increased risk of thrombosis, hemolysis, acute kidney injury, or volume overload [see Warnings and Precautions (5)]. Adequate data on the platelet response to the low dose regimen (e.g. 400 mg/kg per day for 5 consecutive days) are not available for Gammaplex.

    2.3 Administration Hydrate the patient adequately prior to the initiation of infusion. Due to the absence of anti-microbial preservatives, promptly administer Gammaplex after piercing the cap. Infuse Gammaplex intravenously using an intravenous infusion set. See Table 1 for recommended infusion rates. Monitor vital signs throughout the infusion. Slow or stop the infusion if adverse reactions occur. If symptoms subside, the infusion may be resumed at a lower rate that is comfortable for the patient. The observation time of patients after Gammaplex administration may vary. If the patient (a) has not received Gammaplex or another IgG product, (b) is switched from an alternative IGIV product or (c) has had a long interval since the previous infusion, prolong the observation time for adverse reactions after Gammaplex infusion. Certain severe adverse reactions may be related to the rate of infusion. Slowing or stopping the infusion often allows the reaction to disappear. Ensure that patients with pre-existing renal insufficiency are not volume depleted. For patients at increased risk of renal dysfunction, thrombotic events, or volume overload, administer Gammaplex at the minimum infusion rate practicable. Consider discontinuing Gammaplex administration if renal function deteriorates [see Boxed Warning, Warnings and Precautions (5.1, 5.2, 5.8)].