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Relief Hldg Stock Price, News & Analysis

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Company Description

RELIEF THERAPEUTICS Holding SA (OTCQB: RLFTF), historically referred to as Relief Therapeutics, is a commercial-stage biopharmaceutical company focused on rare and debilitating diseases. According to company disclosures, Relief concentrates on select specialty, unmet and rare conditions, with particular emphasis on dermatological, metabolic, and respiratory diseases. The company has highlighted drug delivery systems and drug repurposing as core areas of expertise and has brought several approved products to market through licensing and distribution partnerships.

Relief Therapeutics is headquartered in Geneva, Switzerland and its shares have been listed on the SIX Swiss Exchange under the symbol RLF, while also being quoted in the U.S. on OTCQB under the symbols RLFTF and RLFTY. The company operates in the biopharmaceutical space within the broader manufacturing sector, with activities that span clinical development, regulatory engagement, and commercialization of therapies addressing high unmet medical needs.

Business focus and therapeutic areas

Company communications describe Relief as dedicated to advancing treatment paradigms for rare and debilitating diseases. Its clinical pipeline is said to include treatments targeting rare dermatological conditions, metabolic disorders, and respiratory diseases. Within this framework, Relief has reported work on:

  • RLF-TD011, a highly pure, stabilized hypochlorous acid solution developed with the company’s TEHCLO™ technology, intended for wound care in epidermolysis bullosa (EB), a group of rare, inherited skin disorders characterized by extreme skin fragility and chronic wounds.
  • RLF-OD032, an oral, highly concentrated liquid formulation of sapropterin dihydrochloride for the treatment of phenylketonuria (PKU), a genetic metabolic disorder caused by an inability to properly metabolize phenylalanine.

RLF-TD011 has been described as a sprayable, self-administered solution for targeted wound application, aimed at controlling infection and inflammation while reducing antibiotic use and easing intensive wound care routines. The U.S. Food and Drug Administration (FDA) has granted Orphan Drug and Rare Pediatric Disease designations for RLF-TD011 in EB, and Relief has reported prior clinical experience with its acid-oxidizing solution in non-EB wounds.

For RLF-OD032, Relief has reported positive results from a pivotal bioequivalence clinical study demonstrating bioequivalence to KUVAN® Powder, a reference sapropterin product, under fed conditions. The company characterizes RLF-OD032 as a ready-to-use, portable, highly concentrated liquid that can be administered without water, with the goal of reducing dose volume and potentially improving treatment adherence for individuals living with PKU.

Regulatory interactions and designations

Relief has publicly discussed multiple regulatory interactions related to its pipeline. For RLF-TD011 in EB, the company has noted:

  • Receipt of Orphan Drug Designation from the FDA.
  • Receipt of Rare Pediatric Disease (RPD) designation from the FDA.
  • A constructive pre-Investigational New Drug (pre-IND) meeting with the FDA to clarify remaining clinical and regulatory steps for later-stage development.
  • A determination by the FDA that an initial request for Qualified Infectious Disease Product (QIDP) designation for RLF-TD011 did not meet QIDP criteria, with the company stating that this outcome does not change its development and regulatory strategy for the program.

For RLF-OD032 in PKU, Relief has reported that the pivotal bioequivalence study achieved its primary pharmacokinetic endpoints and that the investigational product was well tolerated, with no serious adverse events reported in the analysis described.

Corporate developments and transformation into MindMaze Therapeutics

In 2025, Relief Therapeutics announced a series of corporate steps leading to a business combination with NeuroX Group SA, a Swiss-based commercial-stage company that had acquired the assets and operations of the legacy MindMaze group. MindMaze had developed digital neurotherapeutics for neurological diseases and brain disorders, delivered via a brain technology platform integrating software, sensors, and telehealth.

According to company announcements, Relief and NeuroX entered into a binding term sheet for a proposed business combination intended to create a publicly listed, AI-based therapeutics platform. Shareholders of Relief subsequently approved resolutions at an extraordinary general meeting authorizing the combination and related capital measures, and the company indicated that it would be renamed MindMaze Therapeutics Holding SA upon completion of the transaction.

Later communications state that the business combination was completed in December 2025, forming MindMaze Therapeutics Holding SA, described as a Swiss-based, commercial-stage company. This combined entity is said to develop and commercialize digital treatments for neurological diseases and brain disorders based on an advanced brain technology platform. It is also reported to manage Relief’s preexisting portfolio of clinical and commercial biopharmaceutical assets focused on rare dermatological, metabolic, and respiratory diseases.

Following completion of the transaction, the company has been described as listed on the SIX Swiss Exchange under the ticker MMTX and quoted in the U.S. on OTCQB under RLFTF and RLFTY. These disclosures indicate that the RLFTF symbol is associated with the combined entity operating as MindMaze Therapeutics Holding SA, while preserving Relief’s historical biopharmaceutical activities within the broader platform.

Position within the healthcare and therapeutics landscape

Based on the company’s own descriptions, Relief Therapeutics’ historical role centers on rare disease biopharmaceutical development, with particular focus on:

  • Rare dermatological conditions, including epidermolysis bullosa.
  • Metabolic disorders such as phenylketonuria.
  • Select respiratory diseases.

With the formation of MindMaze Therapeutics Holding SA through the business combination with NeuroX, the corporate scope described in public communications extends to digital neurotherapeutics and an AI-powered brain health platform, while continuing to manage Relief’s biopharmaceutical asset portfolio. Investors researching RLFTF therefore encounter both the historical Relief Therapeutics biopharmaceutical profile and the newer, combined MindMaze Therapeutics structure as outlined in the company’s press releases.

Frequently asked questions about Relief Therapeutics and RLFTF

Stock Performance

$1.46
0.00%
0.00
Last updated: January 30, 2026 at 11:36
-63.32 %
Performance 1 year
$45.3M

SEC Filings

No SEC filings available for Relief Hldg.

Financial Highlights

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Frequently Asked Questions

What is the current stock price of Relief Hldg (RLFTF)?

The current stock price of Relief Hldg (RLFTF) is $1.46 as of January 30, 2026.

What is the market cap of Relief Hldg (RLFTF)?

The market cap of Relief Hldg (RLFTF) is approximately 45.3M. Learn more about what market capitalization means .

What does Relief Therapeutics Holding SA focus on?

According to its public communications, Relief Therapeutics is a commercial-stage biopharmaceutical company focused on delivering treatment options for select specialty, unmet and rare diseases. Its clinical pipeline targets rare dermatological, metabolic, and respiratory conditions, and the company has highlighted expertise in drug delivery systems and drug repurposing.

Which therapeutic areas are central to Relief Therapeutics’ pipeline?

Company disclosures state that Relief’s pipeline is centered on rare dermatological, metabolic, and respiratory diseases. Examples described in press releases include epidermolysis bullosa, a rare inherited skin disorder, and phenylketonuria, a genetic metabolic condition.

What is RLF-TD011 and what indication is it being developed for?

RLF-TD011 is described by Relief as a highly pure, stabilized hypochlorous acid solution developed using its TEHCLO™ technology. It is being developed as a sprayable, self-administered wound care solution for patients with epidermolysis bullosa, with the goal of controlling infection and inflammation and easing intensive wound care routines.

What regulatory designations has RLF-TD011 received?

Relief reports that the U.S. Food and Drug Administration has granted Orphan Drug Designation and Rare Pediatric Disease designation to RLF-TD011 for the treatment of epidermolysis bullosa. The company has also noted that an initial request for Qualified Infectious Disease Product designation was not granted, but that this did not change its development strategy for the program.

What is RLF-OD032 and how is it intended to help patients with phenylketonuria (PKU)?

RLF-OD032 is described as a ready-to-use, portable, highly concentrated liquid suspension of sapropterin dihydrochloride for oral administration in phenylketonuria. Relief reports that a pivotal bioequivalence study showed RLF-OD032 to be bioequivalent to KUVAN® Powder under fed conditions and that the formulation is designed to reduce dose volume and offer a more patient-friendly treatment option.

Where is Relief Therapeutics based and on which exchanges is it listed?

Company press releases state that Relief Therapeutics is headquartered in Geneva, Switzerland. Its shares have been listed on the SIX Swiss Exchange under the symbol RLF and quoted in the U.S. on OTCQB under the symbols RLFTF and RLFTY.

What business combination did Relief Therapeutics enter into with NeuroX?

Relief announced that it signed a binding term sheet and later completed a business combination with NeuroX Group SA, a Swiss-based commercial-stage company that had acquired the assets and operations of the legacy MindMaze group. The combination was described as creating a publicly listed, AI-based therapeutics platform integrating digital neurotherapeutics with pharmacological treatments.

What is MindMaze Therapeutics Holding SA and how is it related to Relief Therapeutics?

According to company announcements, MindMaze Therapeutics Holding SA is the name of the combined entity formed in December 2025 through the business combination of Relief Therapeutics Holding SA and NeuroX Group SA. The combined company develops and commercializes digital treatments for neurological diseases and brain disorders and manages Relief’s existing portfolio of biopharmaceutical assets.

What does the RLFTF ticker represent after the business combination?

Press releases indicate that following completion of the business combination, MindMaze Therapeutics Holding SA is listed on the SIX Swiss Exchange under the ticker MMTX and is quoted in the U.S. on OTCQB under RLFTF and RLFTY. This associates the RLFTF symbol with the combined entity operating as MindMaze Therapeutics Holding SA while retaining Relief’s historical biopharmaceutical portfolio.

How does Relief describe its approach to rare and debilitating diseases?

Relief describes itself as dedicated to advancing treatment paradigms and improving the lives of patients with rare and debilitating diseases. It emphasizes drug delivery systems, drug repurposing, and the development of therapies that address critical unmet medical needs in rare dermatological, metabolic, and respiratory conditions.