oscar CG096 Multiple Sclerosis Agents

Specifications

• Product Name: Oscar Clinical Guideline: Multiple Sclerosis
• Agents – Medical Benefit Preferred Physician-Administered Drug
• Exceptions Criteria (CG096, Ver. 2)

Product Usage Instructions

Clinical Guidelines Overview
The Oscar Clinical Guideline provides evidence-based clinical criteria for the utilization management of Multiple Sclerosis Agents. The guideline establishes preferred and non-preferred products for physician-administered specialty drugs.

Authorization Process
If you require treatment with a non-preferred product, you need to contact the Plan for authorization. The authorization process involves a coverage review to determine if a clinical exception can be made.

Preferred Drug Selection
Preferred drugs are chosen based on clinical effectiveness, safety, FDA approval, and treatment guidelines. Providers must typically try preferred medications first if they are deemed safe and effective.

Contact Information for Authorization
For Oncology-related requests, contact Ev iCore via their Provider Portal, phone, or fax. For Non-Oncology requests, reach out to Oscar through their Online Portal, phone, or fax.

Frequently Asked Questions (FAQ):

What is the purpose of the Oscar Clinical Guideline?
The guideline aims to establish evidence-based clinical criteria for the utilization management of Multiple Sclerosis Agents.

Oscar Clinical Guideline: Multiple Sclerosis Agents – Medical Benefit Preferred Physician-Administered

Drug Exceptions Criteria (CG096, Ver. 2)
Multiple Sclerosis Agents – Medical Benefit Preferred Physician- Administered Drug Exceptions Criteria

Disclaimer
Clinical guidelines are developed and adopted to establish evidence-based clinical criteria for utilization management decisions. Clinical guidelines are applicable according to policy and plan type. The Plan may delegate utilization management decisions of certain services to third parties who may develop and adopt their own clinical criteria.

Coverage of services is subject to the terms, conditions, and limitations of a member’s policy, as well as applicable state and federal law. Clinical guidelines are also subject to in-force criteria such as the Centers for Medicare & Medicaid Services (CMS) national coverage determination (NCD) or local coverage determination (LCD) for Medicare Advantage plans. Please refer to the member’s policy documents (e.g., Certificate/Evidence of Coverage, Schedule of Benefits, Plan Formulary) or contact the Plan to confirm coverage.

Summary

The Plan has a Medical Preferred Drug List to encourage use of cost-effective and clinically appropriate physician-administered specialty drugs. Table 1 lists the preferred and non-preferred Multiple Sclerosis

Agents
Table 1: Multiple Sclerosis Agents, Medical Preferred Drug List

⇅subject to Plan’s Preferred Physician-Administered Drug(s) Exceptions Criteria.

• Other drug-specific or class-specific clinical guidelines may also be applicable.
• Products considered Formulary or Preferred for the Plan may still require a clinical prior authorization review.
• The Plan may review all requests made under the Medical or Pharmacy benefit against specific prior authorization criteria, as applicable and at its discretion.

This policy outlines the Plan’s preferred products and exception criteria for non-preferred products through prior authorization. The coverage review process will determine if a clinical exception can be made.

• The program applies to all members requesting treatment with a non-preferred product (see Table 1).
• Preferred drugs are selected based on clinical effectiveness, safety, FDA approval, and treatment guidelines. In most cases, preferred medications must be tried first as long as they are considered safe and effective by the provider.
• Requests for non-preferred medications may require meeting Medical Benefit Preferred Drug Exceptions Criteria. Approval may be given if the member has tried and failed, or cannot use the Plan’s preferred drug(s). Exceptions may include, but are not limited to the following:

1. The member has a documented trial and failure, inadequate response, intolerance, or contraindication to ALL preferred drug(s), as applicable; or
2. The member has a risk factor(s) for poor response to the preferred drug(s); or
3. The member is not a candidate for the preferred drug(s) based on the member’s condition(s), individual needs, treatment history, or accepted standards of medical practice.

For more information or to request an exception, please contact the Plan.

Authorization Requirements and Submission Process

Indication Type	Review Entity	Submission Methods	Contact Information
Oncology	EviCore†	Provider Portal	www.evicore.com
		Phone	855-252-1118
		Fax	800-540-2406
Non-Oncology	The Plan (Oscar)	Online Portal	Use the authorization tool at provider.hioscar.com

		Phone	855-672-2755
		Fax	Submit form from www.hioscar.com/forms
Need to check requirements or status? Visit provider.hioscar.com or call 1-855-672-2755

Need to check requirements or status? Visit provider.hioscar.com or call 1-855-672-2755 † EviCore delegation excludes Michigan and California plans, where utilization management decisions are made directly by the Plan or other designated entities per Plan policy. Please refer to Plan-specific documentation for details.

Definitions
“Compendia” are summaries of drug information and medical evidence to support decision-making about the appropriate use of drugs and medical procedures. Examples include, but are not limited to:

1. American Hospital Formulary Service Drug Information
2. Elsevier Clinical Pharmacology
3. National Comprehensive Cancer Network Drugs and Biologics Compendium
4. Thomson Micromedex DrugDex
5. United States Pharmacopeia-National Formulary (USP-NF)

“Contraindication” refers to a pre-existing condition or factor that precludes use of a drug due to risk of harm.
“Intolerance” refers to the inability to tolerate or endure something, often due to experiencing subjectively difficult or harmful side effects, reactions, or hypersensitivities when using a medication or treatment that negatively impacts quality of life, ability to adhere, or overall health. Documentation is expected to detail the specific intolerable effects and their impact on treatment.

“Documentation” refers to written information, including but not limited to:

1. Up-to-date chart notes, relevant test results, and/or relevant imaging reports to support diagnoses;
2. Prescription claims records, and/or prescription receipts to support prior trials of alternatives.

• “Experimental or Investigational“ are procedures, drugs, or devices that haven’t been proven effective or which haven’t been approved by the appropriate regulatory bodies.
• “FDA” refers to the Federal Food and Drug Administration.
• “Medical Benefit Preferred Drug Exceptions Criteria” are Plan requirements that must be met for a non-preferred drug to be approved for coverage, such as trial and failure of preferred drugs first.

State Law Conflicts
For any provision of this policy that directly conflicts with or is prohibited by state law, the provisions of the state law will apply instead of the provisions of this policy. This means that in instances where state regulations diverge from or directly oppose the Plan’s Preferred Physician-Administered Drug(s) Exceptions Criteria or requirements, the policy’s criteria will not apply.

Exception Criteria
The Plan considers a Non-Preferred Product to be medically necessary when the member meets BOTH of the following criteria:

1. Inadequate response, intolerance, or contraindication to ALL FDA, compendia, or evidencebased guideline-supported preferred products that are indicated and clinically appropriate for the diagnosis, unless:
   • There are no such preferred products; or
   • The member is currently receiving treatment with the requested product, excluding when the requested product is obtained as samples or via assistance programs; AND
2. Clinical documentation is provided showing inadequate response, treatment failure, intolerance/adverse event, contraindication or clinical reason to avoid ALL preferred products.
   Examples of supporting documentation include:
   • Office chart notes; and/or
   • Lab results; and/or
   • Diagnostic reports; and/or
   • Clinical summary from provider.
   • If the above prior authorization criteria are met, the requested product will be authorized for up to 12-months.

Experimental or Investigational / Not Medically Necessary

The Plan does not cover non-preferred products when used for experimental, investigational, or medically unnecessary indications. Use of non-preferred products is considered experimental, investigational, or not medically necessary if the indication is outside FDA-approved labeling or not supported by current medical evidence and standards of care. The Plan does not cover non-preferred
products for the following non-approved indications (not all-inclusive):

1.  Uses not considered clinically appropriate based on indication, including age, dosing (dosage, frequency, duration of therapy, and site of administration), and contraindication.
   • Non-FDA approved indications or off label use without sufficient evidence supporting safety and efficacy
   • Doses exceeding the FDA-approved label or clinical practice guidelines without sufficient evidence supporting safety and efficacy
2. Uses not required for treatment or management of the member’s medical condition.
3. Uses not aligned with generally accepted medical practice.
4. Uses primarily for the convenience of the member, family, or provider.

Applicable Billing Codes (HCPCS/CPT Codes)

CPT/HCPCS Codes considered medically necessary if criteria are met:
Code	Description
C9399	Ocrevus Zunovo (ocrelizumab and hyaluronidase-ocsq) Unclassified drugs or biologicals
J0202	Lemtrada Injection, alemtuzumab, 1 mg
J2323	Tysabri Injection, natalizumab, 1 mg
J2350	Ocrevus Injection, ocrelizumab, 1 mg
J2329	Briumvi (ublituximab) Injection, ublituximab-xiiy, 1mg
J3590	Ocrevus Zunovo (ocrelizumab and hyaluronidase-ocsq) Unclassified biologics
Q5134	Injection, natalizumab-sztn (tyruko), biosimilar, 1 mg

References

1. Briumvi (ublituximab) [prescribing information]. Morrisville, NC: TG Therapeutics, Inc; December 2022.
2. Lemtrada (alemtuzumab) [prescribing information]. Cambridge, MA: Genzyme Corporation; May 2023.
3. Ocrevus (ocrelizumab) [prescribing information]. South San Francisco, CA: Genetech Inc; March 2023.
   1. Ocrevus Zunovo (ocrelizumab and hyaluronidase) [prescribing information]. South San Francisco, CA: Genentech Inc; September 2024.
4. Tysabri (natalizumab) [prescribing information]. Cambridge, MA: Biogen Inc; October 2023.

Clinical Guideline Revision / History Information 

Original Date: 12/14/2023
Reviewed/Revised: 12/02/2024

Documents / Resources

oscar CG096 Multiple Sclerosis Agents [pdf] User Guide CG096, CG096 Multiple Sclerosis Agents, Multiple Sclerosis Agents, Sclerosis Agents, Agents

References

• User Manual