Expanded Access Policy

In cases where a clinical trial is not an option, ARMR Sciences, Inc. (“ARMR Sciences”) may elect to provide physician-requested expanded access to its investigational medicines in the U.S. and other countries where ARMR Sciences intends to submit an application for marketing authorization of the requested product. Treating physicians and patients should note that investigational medicines do not have established safety and efficacy, so all potential risks and benefits should be carefully evaluated before seeking expanded access to unapproved medicines. ARMR Sciences will consider requests for access to its investigational medicines, as permitted by applicable law, in very specific circumstances, when all of the following criteria are met:

• The patient has a serious or immediately
• Life-threatening disease for which no alternative therapies are currently available.
• The expanded access program is authorized for the requested indication.
• There is adequate clinical evidence of a positive benefit to risk profile for the investigational medicine in the disease indication, suggesting that a clinically meaningful benefit may be expected and that the benefits outweigh any potential risks.
• Providing investigational medicine through expanded access will not compromise clinical trials or the regulatory pathway.

Physicians seeking expanded access to an ARMR Sciences investigational product on behalf of their patients should submit an inquiry to contact@ARMRSciences.com.

ARMR Sciences will acknowledge receipt of requests from treating physicians, generally within 24-48 hours of receiving the request for information. Physicians will then be directed to submit required documentation to ARMR Sciences.

Professionals at ARMR Sciences who are familiar with the data collected on the investigational drug will evaluate the request based on the scientific evidence available at the time of the request. ARMR Sciences will strive to respond to the treating physician immediately after the receipt of required medical documentation. If ARMR Sciences supports the request for investigational medicine, final approval from regulatory bodies then follows.

Physicians who receive an ARMR Sciences investigational medicine for their patients through the expanded access program must comply with all applicable laws and regulations, contractual conditions, safety reporting required by regulatory agencies, and protection of intellectual property. To view a list of ARMR Science’s open clinical trials, visit Clinicaltrials.gov.

This policy is subject to change. ARMR Sciences will revisit the policy periodically and amend it as appropriate.