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Presentation at ESPGHAN 2026 Describes Additional Groundbreaking Results of Evaluation of Jaguar Health's Crofelemer as Adjunctive Oral Therapy for the Treatment of Pediatric Intestinal Failure (IF)

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Jaguar Health (NASDAQ:JAGX) and family company Napo reported new data at ESPGHAN 2026 on oral liquid crofelemer as adjunctive therapy for pediatric intestinal failure (IF) due to MVID and SBS.

According to Jaguar, long-term treatment showed up to 48% and 40% PS reductions and no significant abnormalities, with a planned NDA filing for MVID in mid‑2027.

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AI-generated analysis. How Rhea-AI works. Not financial advice.

Positive

  • MVID patient showed up to 48% reduction in weekly parenteral support normalized to body weight after >12 months of crofelemer
  • Two pediatric SBS-IF patients showed up to 40% reduction in weekly parenteral support normalized to body weight after >12 months
  • Crofelemer adjunctive therapy reported as well tolerated with no significant clinical or laboratory abnormalities over >12 months
  • Planned NDA filing with the FDA for crofelemer in MVID indication targeted for mid-2027

Negative

  • None.

News Market Reaction – JAGX

+1.35%
1 alert
+1.35% News Effect
+$28K Valuation Impact
$2.06M Market Cap
0.0x Rel. Volume

On the day this news was published, JAGX gained 1.35%, reflecting a mild positive market reaction. This price movement added approximately $28K to the company's valuation, bringing the market cap to $2.06M at that time.

Data tracked by StockTitan Argus on the day of publication.

What This Means

This announcement highlights durable crofelemer benefits with parenteral support cuts of up to 48% i...
Analysis

This announcement highlights durable crofelemer benefits with parenteral support cuts of up to 48% in MVID and 40% in SBS-IF, plus a planned mid-2027 NDA. Investors may watch for regulatory designations and partnering progress as key next steps.

Key Figures

PS reduction (MVID): up to 48% PS reduction (SBS-IF): up to 40% Crofelemer treatment duration: >12 months +5 more
8 metrics
PS reduction (MVID) up to 48% Weekly parenteral support normalized to body weight after >12 months crofelemer
PS reduction (SBS-IF) up to 40% Weekly parenteral support normalized to body weight after >12 months crofelemer
Crofelemer treatment duration >12 months Ongoing oral liquid high-dose crofelemer therapy in pediatric IF patients
Parenteral nutrition duration up to 7 days/week Lifelong total parenteral nutrition required for pediatric IF patients
Daily PS duration up to 20+ hours/day Time on parenteral support for pediatric intestinal failure patients
Planned NDA timing mid-2027 Targeted U.S. FDA NDA filing for crofelemer in MVID indication
ESPGHAN meeting 58th Annual European Society for Pediatric Gastroenterology, Hepatology & Nutrition meeting
E-poster date June 27, 2026 Presentation of exploratory single-arm crofelemer IF trial at ESPGHAN

Historical Context

5 past events · Latest: Jun 25 (Positive)
Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Jun 25 Stock dividend conversion Positive +1.9% Conversion of Series O preferred dividend shares and IF program update.
Jun 23 Regulatory filing Positive -1.9% Completion of New Animal Drug Application for CID in dogs.
Jun 22 Strategic review Positive +19.1% Launch of strategic alternatives review tied to IF NDA plans.
Jun 18 Preclinical data Positive -5.5% Positive preclinical results for coca extract JV program.
Jun 12 Investor presentation Neutral -3.4% Announcement of upcoming investor forum presentation on IF program.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Recent JAGX news has produced mixed but often strong reactions, with both sharp rallies and selloffs around clinical and strategic updates.

Regulatory & Risk Context

Active S-3 Shelf · Short Interest: 7.96%
Shelf Active
Short Interest
7.96% of float
0% 15% 30%+
low as of 2026-06-15 Days to cover: 1.02

Reported short interest appears relatively low, suggesting limited short-squeeze potential and a more typical level of volatility from short covering alone.

Active S-3 Shelf Registration 2025-10-03

An effective S-3 shelf registration gives Jaguar the ability to register and issue securities over time, providing flexibility to raise capital or register resales during the shelf period.

Key Terms

parenteral nutrition, parenteral support, expanded access program, breakthrough therapy designation, +1 more
5 terms
parenteral nutrition medical
"they require lifelong total parenteral nutrition (TPN) with or without supplemental"
Parenteral nutrition is the medical delivery of nutrients and fluids directly into a patient’s bloodstream, usually through an IV, when they cannot eat or absorb food normally—think of it as providing a car with fuel through a hose instead of filling the tank. It matters to investors because it represents a steady, often high-margin product and service line in healthcare; demand, supply chain reliability, regulatory approvals, and reimbursement rates can materially affect revenues and profitability for companies that make or provide these solutions.
parenteral support medical
"with or without supplemental intravenous fluids, which together comprise parenteral support"
Parenteral support is medical care that delivers nutrition, fluids or medications directly into a patient’s bloodstream or body tissues, bypassing the digestive system—think of it as feeding or hydrating someone through an IV rather than by mouth. Investors care because this service involves specialized products, durable revenue from long-term patient use, strict safety and reimbursement rules, and potential regulatory or supply risks that affect company earnings and growth.
expanded access program regulatory
"for the treatment of IF in an infant through an ongoing expanded access program in the U.S."
A program that allows patients with serious or life‑threatening conditions to receive an experimental drug or therapy before it is fully approved by regulators, when they cannot join clinical trials. Investors care because expanded access can change a treatment’s market perception, create early real‑world safety or demand signals, and affect regulatory timelines and potential revenue — like a pre‑order system that also reveals how the product performs outside controlled testing.
breakthrough therapy designation regulatory
"plans to apply for Breakthrough Therapy Designation for crofelemer for the indication of MVID"
A breakthrough therapy designation is a regulatory fast-track given to a drug or treatment that shows early signs of providing a major improvement over existing options for a serious condition. Think of it as a VIP lane that can speed up development and more intensive guidance from regulators, which matters to investors because it can shorten time to market, reduce development risk and potentially increase a company’s value — though it does not guarantee approval.
new drug application regulatory
"with a planned filing of an NDA (New Drug Application) with the U.S. Food and Drug"
A new drug application is a formal request submitted to government regulators seeking approval to market a new medicine. It is like a detailed proposal that shows the drug has been tested for safety and effectiveness. For investors, receiving approval signals that the drug may soon become available for sale, potentially leading to revenue growth and impacting the company's value.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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Company remains sharply focused on its ongoing global development program for crofelemer for rare IF diseases

Near-term milestones for IF program buttressed by continuing groundbreaking results of study, which demonstrate reduction of parenteral support normalized to body weight of up to 48% in patient with the ultrarare pediatric microvillus inclusion disease (MVID)

SAN FRANCISCO, CA / ACCESS Newswire / June 30, 2026 / Jaguar Health, Inc. (NASDAQ: JAGX) ("Jaguar") family company Napo Pharmaceuticals (Napo) today provided a recap of presentations of the oral liquid crofelemer as adjunctive therapy in pediatric intestinal failure (IF) patients at the 58th Annual European Society for Pediatric Gastroenterology, Hepatology & Nutrition (ESPGHAN) Meeting in Lille, France. Napo provided additional data from ongoing investigational studies with oral liquid crofelemer in pediatric patients with IF due to microvillus inclusion disease (MVID) and short bowel syndrome (SBS). Since IF patients cannot orally absorb adequate nutrients, electrolytes and fluids, they require lifelong total parenteral nutrition (TPN) with or without supplemental intravenous fluids, which together comprise parenteral support (PS), for up to seven days per week and up to 20+ hours per day. While PS is supportive, palliative and lifesaving, it is associated with serious complications.

As presented at ESPGHAN 2026, the results of ongoing investigations of liquid oral crofelemer demonstrate substantial reductions of PS and PS normalized to body weight in pediatric IF patients dosed orally for more than one year, with no significant clinical or laboratory abnormalities. In one MVID patient, the weekly PS requirements normalized to body weight have been reduced by up to 48% following >12 months of liquid oral high-dose crofelemer therapy. In two pediatric SBS-IF patients, weekly PS requirements normalized to body weight were reduced up to 40% following >12 months of liquid oral high dose crofelemer therapy.

"Liquid oral crofelemer as adjunctive therapy to PS has been well tolerated with no significant clinical or laboratory abnormalities throughout the ongoing treatment period of >12 months in these pediatric IF patients with MVID or SBS. In addition, the reductions in weekly PS requirements normalized to body weight with excellent tolerability support the continued development of liquid oral crofelemer as the first oral adjunctive therapy for pediatric intestinal failure patients receiving lifelong PS," said Dr. Pravin Chaturvedi, Chair of Scientific Advisory Board and Chief Scientific Officer of Napo and Jaguar.

"We remain sharply focused on and committed to our global development program for our novel liquid oral crofelemer formulation as adjunctive treatment for the management of rare IF conditions such as MVID and SBS," said Lisa Conte, Jaguar's founder, president, and CEO. "Our IF program is expected to continue to provide clinical milestones and is the subject of business development discussions with the potential to bring in non-dilutive funds from potential licensee partners. If appropriate, Jaguar plans to apply for Breakthrough Therapy Designation for crofelemer for the indication of MVID, with a planned filing of an NDA (New Drug Application) with the U.S. Food and Drug Administration (FDA) for this indication in mid-2027."

One e-poster was presented on June 27, 2026 at ESPGHAN titled Exploratory Single-Arm, Open-Label Non-Randomized Trial Evaluating the Safety and Effectiveness of Crofelemer in Pediatric Patients with Intestinal Failure, and the associated abstract can be viewed by clicking here.

Another report of the evaluation of novel liquid oral crofelemer adjunctive therapy, for the treatment of IF in an infant through an ongoing expanded access program in the U.S., was presented for e-poster viewing at ESPGHAN 2026. The study demonstrated that total daily parenteral nutrition volume and caloric delivery remained stable throughout crofelemer therapy despite ongoing growth, while stool output was simultaneously reduced. The abstract, titled Crofelemer for Symptom Management in Microvillus Inclusion Disease: A Case Report in an Infant, can be viewed by clicking here.

The European Society for Pediatric Gastroenterology Hepatology and Nutrition (ESPGHAN) is a multi-professional organization whose aim is to promote the health of children with special attention to the gastrointestinal tract, liver and nutritional status, through knowledge creation, the dissemination of science based information, the promotion of best practice in the delivery of care and the provision of high quality education for pediatric gastroenterology, hepatology and nutrition professionals in Europe and beyond.

About Crofelemer

Crofelemer is a novel, oral plant-based prescription medicine purified from the red bark sap, also referred to as "dragon's blood," of the Croton lechleri tree in the Amazon Rainforest. Napo Pharmaceuticals has established a sustainable harvesting program, under fair trade practices, for crofelemer to ensure a high degree of quality, ecological integrity, and support for indigenous communities.

About the Jaguar Health Family of Companies

Jaguar Health, Inc. (Jaguar) is a commercial stage pharmaceuticals company focused on developing novel proprietary prescription medicines sustainably derived from plants from rainforest areas for people and animals with gastrointestinal distress. Jaguar family companies Napo Pharmaceuticals, Inc. (Napo) and Napo Therapeutics S.p.A. focus on the development and commercialization of novel crofelemer powder for oral solution for the treatment of rare and orphan gastrointestinal disorders with intestinal failure, including microvillus inclusion disease and short bowel syndrome.

For more information about:

Jaguar Health, visit https://jaguar.health

Napo Pharmaceuticals, visit napopharma.com

Napo Therapeutics, visit napotherapeutics.com

Forward-Looking Statements

Certain statements in this press release constitute "forward-looking statements." These include statements regarding Jaguar's expectation that its intestinal failure program will continue to provide clinical milestones, Jaguar's expectation that the opportunity may exist to bring in non-dilutive funds from potential licensee partners to support the intestinal failure program, Jaguar's plans to pursue Breakthrough Therapy designation for crofelemer for the indication of MVID, and Jaguar's expectation that the company will file an NDA with the FDA for the MVID indication in mid-2027. In some cases, you can identify forward-looking statements by terms such as "may," "will," "should," "expect," "plan," "aim," "anticipate," "could," "intend," "target," "project," "contemplate," "believe," "estimate," "predict," "potential" or "continue" or the negative of these terms or other similar expressions. The forward-looking statements in this release are only predictions. Jaguar has based these forward-looking statements largely on its current expectations and projections about future events. These forward-looking statements speak only as of the date of this release and are subject to several risks, uncertainties, and assumptions, some of which cannot be predicted or quantified and some of which are beyond Jaguar's control. Except as required by applicable law, Jaguar does not plan to publicly update or revise any forward-looking statements contained herein, whether as a result of any new information, future events, changed circumstances or otherwise.

Contact:
hello@jaguar.health
Jaguar-JAGX

SOURCE: Jaguar Health, Inc.



View the original press release on ACCESS Newswire

FAQ

What new crofelemer results did Jaguar Health (JAGX) present at ESPGHAN 2026?

Jaguar Health reported long-term crofelemer data showing reduced parenteral support needs in pediatric intestinal failure. According to Jaguar, MVID and SBS patients on oral liquid crofelemer for over 12 months experienced meaningful reductions in weekly parenteral support normalized to body weight.

How much did crofelemer reduce parenteral support in pediatric MVID patients for JAGX?

In one pediatric MVID patient, crofelemer reduced weekly parenteral support normalized to body weight by up to 48%. According to Jaguar, this reduction followed more than 12 months of high-dose liquid oral crofelemer therapy as adjunctive treatment to lifelong parenteral support.

What were the crofelemer results in pediatric short bowel syndrome (SBS-IF) for Jaguar Health?

Two pediatric SBS-IF patients showed up to 40% reductions in weekly parenteral support normalized to body weight. According to Jaguar, these reductions occurred after more than 12 months of high-dose liquid oral crofelemer used alongside standard parenteral support therapy.

How well was Jaguar Health’s crofelemer tolerated in pediatric intestinal failure patients?

Crofelemer was reported as well tolerated in pediatric MVID and SBS intestinal failure patients treated for over 12 months. According to Jaguar, there were no significant clinical or laboratory abnormalities during ongoing adjunctive therapy with liquid oral crofelemer.

What regulatory plans does Jaguar Health (JAGX) have for crofelemer in MVID?

Jaguar plans to apply for Breakthrough Therapy Designation and file an NDA for crofelemer in MVID. According to Jaguar, the New Drug Application submission to the FDA is planned for mid-2027, subject to appropriate conditions being met.

What did the expanded access case report of crofelemer in an infant with MVID show?

The infant case report showed stable daily parenteral nutrition volume and calories during crofelemer therapy despite growth. According to Jaguar, stool output was reduced, suggesting potential symptom management benefits in microvillus inclusion disease within an expanded access setting.

How does crofelemer fit into treatment of pediatric intestinal failure patients on lifelong parenteral support?

Crofelemer is being evaluated as adjunctive oral therapy to lifelong parenteral support in rare IF conditions. According to Jaguar, reductions in parenteral support needs and favorable tolerability support continued development as a potential first oral adjunctive option for these patients.