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Napo Pharmaceuticals

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uuid00009ju

Namestring
Napo Pharmaceuticals
Legal namestring
Napo Pharmaceuticals, Inc.
Websiteurl
napopharma.com
Company typeenum
Private
Founded yearint
2017
Descriptiontext

Napo Pharmaceuticals, Inc. is a San Francisco-based, privately held pharmaceutical company and wholly-owned subsidiary of Jaguar Health, Inc. (NASDAQ: JAGX) that develops and commercializes proprietary, plant-based gastrointestinal drugs for supportive care and rare intestinal diseases. Its core asset is crofelemer, an FDA-approved first-in-class botanical drug extracted from the sustainably harvested Croton lechleri (sangre de drago) tree sap, which works through a novel mechanism of inhibitory modulation of two secretory chloride ion channels in the gut. The commercial portfolio includes Mytesi for noninfectious diarrhea in adults with HIV/AIDS on antiretroviral therapy, Canalevia-CA1 for chemotherapy-induced diarrhea in dogs, and Gelclair for oral mucositis in cancer patients, while the pipeline targets cancer therapy-related diarrhea (Phase 3 OnTarget), rare pediatric intestinal failure indications including microvillus inclusion disease and short bowel syndrome with intestinal failure (orphan drug designation in the US and EU), and infectious diarrhea via NP-300.

Napo generates revenue through a hybrid model combining product sales, out-licensing, and milestone payments. In January 2026 the company entered an exclusive US licensing agreement with Future Pak for Mytesi and Canalevia-CA1, receiving an upfront payment plus milestones and transferring commercialization while retaining manufacturing; this drove consolidated revenue to $20.2M in Q1 2026, versus $3.24M in Q4 2025. The company's go-to-market combines medical conference engagement (ESPGHAN, NASPGHAN, ONS), an investigator-initiated trial program in academic centers across the US, Germany, Italy, and the UAE, and a dedicated Mytesi call center; a parallel Italian subsidiary, Napo Therapeutics S.P.A., runs the SBS-IF clinical program in Europe. Operationally the company operates with 11-50 employees and is also exploring broader strategic alternatives at the Jaguar Health parent level.

Short descriptiontext

Napo Pharmaceuticals is a San Francisco-based Jaguar Health subsidiary that develops plant-based gastrointestinal drugs, led by FDA-approved crofelemer (Mytesi) for HIV/AIDS-related diarrhea, with pipeline programs in cancer therapy-related diarrhea and rare pediatric intestinal failure diseases such as MVID and SBS-IF.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1–10
akta.pro rankint
HeadquartersSan Francisco, United States
HQ citystring
San Francisco
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
botanical pharmaceuticals, gastrointestinal therapeutics, rare disease drugs, plant-based medicines, prescription drug development
Industry1 code
1Gastroenterology Specialty Pharmaceuticals
CodeHLAIACAEPrimaryYes
NAICS code2 codes
  • Pharmaceutical Preparation Manufacturing325412
  • Medicinal and Botanical Manufacturing325411
SIC code2 codes
  • Pharmaceutical Preparations2834
  • Medicinal Chemicals & Botanical Products2833
Product category
Specialty Pharmaceuticals
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model4 records
1Mytesi Sales
TypeOne Time License
Description

Sales of FDA-approved Mytesi (crofelemer) for symptomatic relief of noninfectious diarrhea in adults with HIV/AIDS on antiretroviral therapy. Licensed exclusively to Future Pak for US commercialization while Napo retains manufacturing.

in.investing.com
2Canalevia-CA1 Sales
TypeOne Time License
Description

Sales of FDA-approved Canalevia-CA1 for chemotherapy-induced diarrhea in dogs. Licensed exclusively to Future Pak for US commercialization.

in.investing.com
3Licensing Milestone Payments
TypeLicensing Royalties
Description

Potential milestone payments from Future Pak licensing agreement up to $20 million. Received $16 million upfront and $3 million additional payment in early 2026.

investing.com
4Strategic Licensing Agreement
TypeLicensing Royalties
Description

January 2026 licensing agreement with Future Pak generating $18 million upfront plus potential milestones; resulted in 816% revenue surge to $20.2 million in Q1 2026.

in.investing.com
Marketing channels4 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels3 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Personnel, Technology or R&D, Supply Chain, Marketing or Sales, Operations
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 3 records shown
1Mytesi
Description

FDA-approved prescription drug (crofelemer) for symptomatic relief of noninfectious diarrhea in adults living with HIV/AIDS on antiretroviral therapy

napopharma.com
+2 more records
Core offering1 text field

Napo Pharmaceuticals develops and commercializes proprietary, plant-based prescription pharmaceuticals derived from Croton lechleri (sangre de drago) tree sap, with its lead compound crofelemer approved for symptomatic relief of noninfectious diarrhea in HIV/AIDS adults and in development for cancer therapy-related diarrhea and rare pediatric intestinal failure disorders (MVID, SBS-IF). The company is a wholly-owned subsidiary of Jaguar Health and operates a licensing-based commercial model.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 3 values shown
  • Parenteral support reduction of 12-37% in pediatric intestinal failure patients
+2 more records
Product overview1 text field

Napo Pharmaceuticals is a wholly-owned subsidiary of Jaguar Health that develops and commercializes proprietary, plant-based gastrointestinal pharmaceuticals. Their core product portfolio includes Mytesi (crofelemer), an FDA-approved delayed-release tablet for noninfectious diarrhea in HIV/AIDS patients, and Canalevia-CA1 for veterinary use. The company is actively developing crofelemer in multiple formulations and indications including: powder for oral solution targeting rare pediatric conditions like microvillus inclusion disease (MVID) and short bowel syndrome with intestinal failure (SBS-IF); and the OnTarget Phase 3 trial for cancer therapy-related diarrhea (CTD). Additional products include Gelclair for oral mucositis and NP-300 for infectious diarrhea. All lead products are derived from the Croton lechleri tree (sangre de drago) harvested from rainforest regions using sustainable practices.

Product and service1 record
1Mytesi (crofelemer)
Scale indicator8 records

Each record includes

Type, Value, Description, Source

Partnership4 partners
Strategic tierCoreTypeChannel Partner/ Reseller/ DistributorAnnounced on2026-01-01
Description

January 2026 licensing agreement making Future Pak the exclusive marketer of Mytesi and Canalevia-CA1 in the US. Napo received $16 million upfront and $3 million additional payment; up to $20 million in milestone payments remaining. Napo retains manufacturing responsibilities while Future Pak handles commercialization beyond the initial five-year period.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Independent investigator-initiated proof-of-concept study of crofelemer liquid formulation in pediatric intestinal failure patients conducted at Sheikh Khalifa Medical City in Abu Dhabi, UAE. Study demonstrated parenteral support reductions of 12-37% in MVID and SBS patients with patients on treatment for more than one year.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Italian corporation established by Jaguar Health in 2021 focused on rare disease indications for crofelemer. Led by rare-disease management professionals. Currently enrolling adult SBS-IF patients in randomized double-blind placebo-controlled trial at sites in Germany and Italy.

Strategic tierMinorTypeChannel Partner/ Reseller/ Distributor
Description

Product inventory sales arrangement for Napo products; $1.0 million received in April 2026 as part of non-dilutive capital improvement.

Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers8 records
TypeEmerging player
Description

Clinical-stage biotech with oral peptide platform addressing hypoparathyroidism and metabolic bone disease; comparable as a small-cap, pipeline-focused therapeutics company with a niche specialty pharma profile.

TypeBroad incumbent
Description

GI-focused specialty pharma (now part of Bausch Health) with a broad portfolio of prescription GI products; comparable as a leading prescription GI therapeutics franchise targeting similar physician specialties.

3Synthetic Biologics
TypeEmerging player
Description

Clinical-stage biotech developing anti-infective and GI therapeutics including treatments for C. difficile and chemotherapy-induced diarrhea; comparable given shared focus on supportive care in oncology and infectious GI disease.

TypeDirect peer
Description

Commercial-stage GI specialty pharma with novel mechanism drugs (tenapanor for IBS-C and hyperphosphatemia); highly comparable as a small-cap, mechanism-focused GI therapeutics developer pursuing niche indications.

TypeDirect peer
Description

Private GI specialty pharma developing treatments for IBS, chronic constipation, and rare GI conditions; comparable as a privately-held GI therapeutics developer focused on supportive care and niche indications.

TypeDirect peer
Description

GI specialty pharma behind Linzess (linaclotide) for IBS-C and chronic constipation; comparable business model of developing and commercializing novel-mechanism GI drugs for chronic conditions.

TypeBroad incumbent
Description

Parent company of Napo Pharmaceuticals and developer of Mytesi/Crofelemer at the corporate level; included as the immediate corporate parent and animal-health-focused sponsor of Napo's human pharma pipeline.

TypeBroad incumbent
Description

Specialty pharma with a gastroenterology portfolio (e.g., Amitiza) and rare disease focus; comparable as a larger specialty pharma with overlap in GI and rare disease therapeutics.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat5 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights6 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers4 records

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment5 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile3 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
No
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature3 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles3 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

Subsidiaries1 record

Each record includes

Name, Acquired on, Relationship type, Type, Business focus

No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds7 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors3 records

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Napo Pharmaceuticals

Specialty Pharmaceuticalsnapopharma.com

Napo Pharmaceuticals is a San Francisco-based Jaguar Health subsidiary that develops plant-based gastrointestinal drugs, led by FDA-approved crofelemer (Mytesi) for HIV/AIDS-related diarrhea, with pipeline programs in cancer therapy-related diarrhea and rare pediatric intestinal failure diseases such as MVID and SBS-IF.

What Napo Pharmaceuticals does

Napo Pharmaceuticals, Inc. is a San Francisco-based, privately held pharmaceutical company and wholly-owned subsidiary of Jaguar Health, Inc. (NASDAQ: JAGX) that develops and commercializes proprietary, plant-based gastrointestinal drugs for supportive care and rare intestinal diseases. Its core asset is crofelemer, an FDA-approved first-in-class botanical drug extracted from the sustainably harvested Croton lechleri (sangre de drago) tree sap, which works through a novel mechanism of inhibitory modulation of two secretory chloride ion channels in the gut. The commercial portfolio includes Mytesi for noninfectious diarrhea in adults with HIV/AIDS on antiretroviral therapy, Canalevia-CA1 for chemotherapy-induced diarrhea in dogs, and Gelclair for oral mucositis in cancer patients, while the pipeline targets cancer therapy-related diarrhea (Phase 3 OnTarget), rare pediatric intestinal failure indications including microvillus inclusion disease and short bowel syndrome with intestinal failure (orphan drug designation in the US and EU), and infectious diarrhea via NP-300.

Napo generates revenue through a hybrid model combining product sales, out-licensing, and milestone payments. In January 2026 the company entered an exclusive US licensing agreement with Future Pak for Mytesi and Canalevia-CA1, receiving an upfront payment plus milestones and transferring commercialization while retaining manufacturing; this drove consolidated revenue to $20.2M in Q1 2026, versus $3.24M in Q4 2025. The company's go-to-market combines medical conference engagement (ESPGHAN, NASPGHAN, ONS), an investigator-initiated trial program in academic centers across the US, Germany, Italy, and the UAE, and a dedicated Mytesi call center; a parallel Italian subsidiary, Napo Therapeutics S.P.A., runs the SBS-IF clinical program in Europe. Operationally the company operates with 11-50 employees and is also exploring broader strategic alternatives at the Jaguar Health parent level.

Napo Pharmaceuticals firmographics

Firmographics
Name
Napo Pharmaceuticals
Legal name
Napo Pharmaceuticals, Inc.
Website
https://napopharma.com
Company type
Private
Founded year
2017
Operating status
Operating
Headcount range
1–10 employees
Short description
Napo Pharmaceuticals is a San Francisco-based Jaguar Health subsidiary that develops plant-based gastrointestinal drugs, led by FDA-approved crofelemer (Mytesi) for HIV/AIDS-related diarrhea, with pipeline programs in cancer therapy-related diarrhea and rare pediatric intestinal failure diseases such as MVID and SBS-IF.
Ownership category
akta.pro rank

Napo Pharmaceuticals industry classification

Industry
Product category
Specialty Pharmaceuticals
NAICS
Pharmaceutical Preparation Manufacturing (325412), Medicinal and Botanical Manufacturing (325411)
SIC
Pharmaceutical Preparations (2834), Medicinal Chemicals & Botanical Products (2833)
akta.pro primary industry
Gastroenterology Specialty Pharmaceuticals (HLAIACAE)

Keywords

  • Botanical pharmaceuticals
  • Gastrointestinal therapeutics
  • Rare disease drugs
  • Plant-based medicines
  • Prescription drug development

Where Napo Pharmaceuticals is headquartered

Location

Headquarters

HQ city
San Francisco
HQ country
United States
HQ region
North America

Offices1 record

Markets served

Napo Pharmaceuticals business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Personnel, Technology or R&D, Supply Chain, Marketing or Sales, Operations

Revenue model

  1. Mytesi Sales: Sales of FDA-approved Mytesi (crofelemer) for symptomatic relief of noninfectious diarrhea in adults with HIV/AIDS on antiretroviral therapy. Licensed exclusively to Future Pak for US commercialization while Napo retains manufacturing.
  2. Canalevia-CA1 Sales: Sales of FDA-approved Canalevia-CA1 for chemotherapy-induced diarrhea in dogs. Licensed exclusively to Future Pak for US commercialization.
  3. Licensing Milestone Payments: Potential milestone payments from Future Pak licensing agreement up to $20 million. Received $16 million upfront and $3 million additional payment in early 2026.
  4. Strategic Licensing Agreement: January 2026 licensing agreement with Future Pak generating $18 million upfront plus potential milestones; resulted in 816% revenue surge to $20.2 million in Q1 2026.

Go-to-market motion2 records

Distribution channels3 records

Marketing channels4 records

Napo Pharmaceuticals product offering

Product offering

Core offering

Napo Pharmaceuticals develops and commercializes proprietary, plant-based prescription pharmaceuticals derived from Croton lechleri (sangre de drago) tree sap, with its lead compound crofelemer approved for symptomatic relief of noninfectious diarrhea in HIV/AIDS adults and in development for cancer therapy-related diarrhea and rare pediatric intestinal failure disorders (MVID, SBS-IF). The company is a wholly-owned subsidiary of Jaguar Health and operates a licensing-based commercial model.

Product overview

Napo Pharmaceuticals is a wholly-owned subsidiary of Jaguar Health that develops and commercializes proprietary, plant-based gastrointestinal pharmaceuticals. Their core product portfolio includes Mytesi (crofelemer), an FDA-approved delayed-release tablet for noninfectious diarrhea in HIV/AIDS patients, and Canalevia-CA1 for veterinary use. The company is actively developing crofelemer in multiple formulations and indications including: powder for oral solution targeting rare pediatric conditions like microvillus inclusion disease (MVID) and short bowel syndrome with intestinal failure (SBS-IF); and the OnTarget Phase 3 trial for cancer therapy-related diarrhea (CTD). Additional products include Gelclair for oral mucositis and NP-300 for infectious diarrhea. All lead products are derived from the Croton lechleri tree (sangre de drago) harvested from rainforest regions using sustainable practices.

Differentiator

Problem solved

Functional benefit

Brands

  • Mytesi: FDA-approved prescription drug (crofelemer) for symptomatic relief of noninfectious diarrhea in adults living with HIV/AIDS on antiretroviral therapy
  • Canalevia-CA1
  • Gelclair

Products and services

  • Mytesi (crofelemer)

Quantifiable outcome

  • Parenteral support reduction of 12-37% in pediatric intestinal failure patients
  • +2 more outcomes

Companies that use Napo Pharmaceuticals

Customer profile

Named customers4 records

Segments5 records

Ideal customer profiles3 records

Napo Pharmaceuticals technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature3 records

Napo Pharmaceuticals partnerships and signals

Strategic signal

Partnerships

Four partnerships are on record, tiered core and minor.

  • Future Pak, LLCcoreChannel Partner/ Reseller/ Distributor · 1 January 2026January 2026 licensing agreement making Future Pak the exclusive marketer of Mytesi and Canalevia-CA1 in the US. Napo received $16 million upfront and $3 million additional payment; up to $20 million in milestone payments remaining. Napo retains manufacturing responsibilities while Future Pak handles commercialization beyond the initial five-year period.
  • Sheikh Khalifa Medical CitycoreStrategic or Co-development PartnerIndependent investigator-initiated proof-of-concept study of crofelemer liquid formulation in pediatric intestinal failure patients conducted at Sheikh Khalifa Medical City in Abu Dhabi, UAE. Study demonstrated parenteral support reductions of 12-37% in MVID and SBS patients with patients on treatment for more than one year.
  • Napo Therapeutics S.P.A.coreStrategic or Co-development PartnerItalian corporation established by Jaguar Health in 2021 focused on rare disease indications for crofelemer. Led by rare-disease management professionals. Currently enrolling adult SBS-IF patients in randomized double-blind placebo-controlled trial at sites in Germany and Italy.
  • Woodward Specialty LLCminorChannel Partner/ Reseller/ DistributorProduct inventory sales arrangement for Napo products; $1.0 million received in April 2026 as part of non-dilutive capital improvement.

Scale indicators8 records

Recent moves7 records

Expansion highlights6 records

Napo Pharmaceuticals competitors and assessment

Company assessment

Emerging players

  • Entera Bio: Clinical-stage biotech with oral peptide platform addressing hypoparathyroidism and metabolic bone disease; comparable as a small-cap, pipeline-focused therapeutics company with a niche specialty pharma profile.
  • Synthetic Biologics: Clinical-stage biotech developing anti-infective and GI therapeutics including treatments for C. difficile and chemotherapy-induced diarrhea; comparable given shared focus on supportive care in oncology and infectious GI disease.

Broad incumbents

  • Salix Pharmaceuticals: GI-focused specialty pharma (now part of Bausch Health) with a broad portfolio of prescription GI products; comparable as a leading prescription GI therapeutics franchise targeting similar physician specialties.
  • Jaguar Health: Parent company of Napo Pharmaceuticals and developer of Mytesi/Crofelemer at the corporate level; included as the immediate corporate parent and animal-health-focused sponsor of Napo's human pharma pipeline.
  • Mallinckrodt Pharmaceuticals: Specialty pharma with a gastroenterology portfolio (e.g., Amitiza) and rare disease focus; comparable as a larger specialty pharma with overlap in GI and rare disease therapeutics.

Direct peers

  • Ardelyx: Commercial-stage GI specialty pharma with novel mechanism drugs (tenapanor for IBS-C and hyperphosphatemia); highly comparable as a small-cap, mechanism-focused GI therapeutics developer pursuing niche indications.
  • Sebela Pharmaceuticals: Private GI specialty pharma developing treatments for IBS, chronic constipation, and rare GI conditions; comparable as a privately-held GI therapeutics developer focused on supportive care and niche indications.
  • Ironwood Pharmaceuticals: GI specialty pharma behind Linzess (linaclotide) for IBS-C and chronic constipation; comparable business model of developing and commercializing novel-mechanism GI drugs for chronic conditions.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat5 records

Key risks6 records

Key highlights6 records

Customer concentration

Napo Pharmaceuticals social profiles

Digital presence

Napo Pharmaceuticals financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Napo Pharmaceuticals leadership team

Management profile

Number of profiles

Profiles3 records

Napo Pharmaceuticals subsidiaries and ownership

Company hierarchy

Subsidiaries1 record

Napo Pharmaceuticals funding detail

Funding detail

Funding overview

Funding rounds7 records

Investors3 records

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Napo Pharmaceuticals M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Napo Pharmaceuticals

What does Napo Pharmaceuticals do?

Napo Pharmaceuticals develops and commercializes proprietary, plant-based prescription pharmaceuticals derived from Croton lechleri (sangre de drago) tree sap, with its lead compound crofelemer approved for symptomatic relief of noninfectious diarrhea in HIV/AIDS adults and in development for cancer therapy-related diarrhea and rare pediatric intestinal failure disorders (MVID, SBS-IF). The company is a wholly-owned subsidiary of Jaguar Health and operates a licensing-based commercial model.

Is Napo Pharmaceuticals a public or private company?

Napo Pharmaceuticals is a private company. It is classified as corporate owned and is currently operating.

When was Napo Pharmaceuticals founded?

Napo Pharmaceuticals was founded in 2017. It employs 1 to 10 people.

Where is Napo Pharmaceuticals based?

Napo Pharmaceuticals is headquartered in San Francisco, United States, in the North America region.

How does Napo Pharmaceuticals make money?

Four revenue lines are on record. Mytesi Sales are the primary driver. The others are canalevia-CA1 Sales, licensing Milestone Payments and strategic Licensing Agreement.

Who are Napo Pharmaceuticals's main competitors?

Emerging players on record are Entera Bio and Synthetic Biologics. Broad incumbents are Salix Pharmaceuticals, Jaguar Health and Mallinckrodt Pharmaceuticals. Direct peers are Ardelyx, Sebela Pharmaceuticals and Ironwood Pharmaceuticals.

Does Napo Pharmaceuticals have an API?

No public API is recorded for Napo Pharmaceuticals.

What industry is Napo Pharmaceuticals in?

Napo Pharmaceuticals's product category is Specialty Pharmaceuticals. Its primary akta.pro industry code is HLAIACAE, Gastroenterology Specialty Pharmaceuticals. Its NAICS code is 325412 and its SIC code is 2834.

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Live signals
Stock TitanJaguar Health's Napo sponsors intestinal failure panelNapo Pharmaceuticals, a Jaguar Health family company, is sponsoring a panel on intestinal failure at the 2nd Best of Elite Ped-GI meeting in Abu Dhabi on October 30, 2026. Ongoing pediatric crofelemer trials show substantial reductions in parenteral nutrition needs with no significant clinical or laboratory abnormalities. Jaguar plans to file a New Drug Application for MVID in mid-2027.Stock TitanJaguar Health Crofelemer Abstract Accepted for ACG 2026Jaguar Health's Napo Pharmaceuticals accepted an abstract on preliminary results of an open-label study of crofelemer in adult short bowel syndrome patients with intestinal failure for ACG 2026. The company expects results from a separate controlled Phase 2 trial in adult Type 1 SBS patients early in the second half of 2027.YahooJaguar Health Receives Fee Waivers from FDAJaguar Health's Napo Pharmaceuticals received FDA fee waivers for Mytesi and Canalevia-CA1 for the 2027 fiscal year. The waivers cover the Prescription Drug User Fee Act and the Center for Veterinary Medicine. Jaguar remains focused on its MVID and SBS development program, targeting an NDA filing for MVID mid-2027.YahooAdditional Infant Patient to Receive Jaguar Health's Crofelemer for Compassionate Use for Treatment of Intestinal Failure (IF)Jaguar Health announced that Napo Pharmaceuticals is providing crofelemer powder for an infant with congenital sodium diarrhea, using it as adjunctive therapy to parenteral support. Ongoing studies show up to 48% reduction in weekly parenteral support needs for MVID patients and up to 40% for SBS-IF patients. Jaguar plans to file an NDA for MVID in mid-2027.Stock TitanJaguar Health Provides Crofelemer for Infant UseJaguar Health announced that Napo Pharmaceuticals is providing crofelemer to an infant with congenital sodium diarrhea, an intestinal failure condition. The company plans to file an NDA for microvillus inclusion disease in mid-2027, with ongoing studies showing up to 48% reduction in parenteral support needs.The Pharma LetterJaguar Health progresses crofelemer for rare intestinal failure disordersNapo Pharmaceuticals, a Jaguar Health company, is providing its novel crofelemer powder for oral solution to treat intestinal failure in an infant with congenital sodium diarrhea caused by a GUCY2C gene mutation. The condition presents significant challenges in managing nutritional and electrolyte deficiencies, particularly in pediatric patients.FinancialContent Business PageJaguar Health Satisfies Conditions for Receipt of Non-Dilutive $2 Million Holdback Payment from Future Pak for Commercial License to Mytesi and Canalevia-CA1Jaguar Health's wholly-owned subsidiary Napo Pharmaceuticals has satisfied conditions required to receive a $2 million holdback payment from Future Pak, LLC related to the U.S. commercial licensing agreement for Mytesi and Canalevia-CA1, crofelemer-based drugs. The company previously received $16 million upfront in January 2026 and an additional $3 million in March 2026, with up to $17 million in additional milestone payments still possible. Jaguar is now focusing its crofelemer development on rare intestinal failure conditions, including planning to file an NDA for MVID indication in mid-2027 and pursuing Breakthrough Therapy Designation.Investing.comJaguar unit provides crofelemer to EU infant for rare disease By Investing.comJaguar Health Inc.'s subsidiary Napo Pharmaceuticals is providing crofelemer powder for oral solution to an infant in the European Union for compassionate use treatment of microvillus inclusion disease, a rare intestinal failure condition affecting approximately 200 patients worldwide. Clinical trial data presented at a pediatric gastroenterology conference showed reductions in parenteral support requirements of up to 48% in one patient and up to 40% in two short bowel syndrome patients after more than 12 months of treatment. The company has completed enrollment in its pivotal clinical trial and plans to apply for Breakthrough Therapy Designation and file a New Drug Application with the FDA in mid-2027.AInvestJaguar Health - Napo and Alivus enter new manufacturing and supply agreement for crofelemer on July 9, 2026 - SEC filingNapo, a subsidiary of Jaguar Health, and Alivus entered into a new manufacturing and supply agreement for crofelemer on July 9, 2026, as disclosed in an SEC filing. The article provides no details on the terms, duration, or financial implications of the agreement.FinancialContent Business PagePresentation 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)Napo Pharmaceuticals, a family company of Jaguar Health, presented additional clinical data at the 58th Annual ESPGHAN Meeting in Lille, France, showing that liquid oral crofelemer as adjunctive therapy significantly reduced parenteral support requirements by up to 48% in a pediatric MVID patient and up to 40% in two pediatric SBS-IF patients after more than 12 months of treatment. The ongoing studies demonstrated substantial PS reductions with no significant clinical or laboratory abnormalities in pediatric intestinal failure patients. Jaguar plans to pursue Breakthrough Therapy Designation from the FDA and file a New Drug Application for the MVID indication in mid-2027.