iBio, Inc. (IBIO) Business Model Canvas

IBIO, Inc. (IBIO): Business Model Canvas [Jan-2025 Mise à jour]

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Dans le monde dynamique de la biotechnologie, Ibio, Inc. (IBIO) émerge comme une force pionnière, révolutionnant la fabrication pharmaceutique grâce à sa révolutionnaire FastPharming® plate-forme. En exploitant la puissance de la production de protéines à base de plantes, cette entreprise innovante transforme la façon dont les vaccins et les biologiques sont développés, offrant une solution durable, évolutive et rentable qui promet de remodeler l'avenir de la recherche médicale et de la production de médicaments. Plongez dans les subtilités du modèle commercial unique d'Ibio, où l'innovation scientifique rencontre l'entrepreneuriat stratégique.


IBIO, Inc. (IBIO) - Modèle commercial: partenariats clés

Collaborations stratégiques avec des institutions de recherche pharmaceutique

En 2024, IBIO, Inc. maintient des partenariats de recherche stratégiques avec les institutions suivantes:

Institution Focus de partenariat Statut de collaboration
Texas A&M AgriLife Research Développement de protéines à base de plantes Actif
Université d'État de Caroline du Nord Recherche de biotechnologie Actif

Partenariats de fabrication contractuels

Les collaborations de fabrication de contrats d'IBIO incluent:

  • Partenariat de fabrication confirmé avec les services de fabrication de contrats biopharmatiques
  • Collaboration continue avec Fraunhofer Center for Molecular Biotechnology

Partenariats de recherche universitaire

Établissement universitaire Domaine de recherche Montant du financement
Université de Californie, Davis Ingénierie des protéines à base de plantes $750,000
Université du Maryland Technologie vectorielle virale $450,000

Accords de licence

Accords de licence de technologie propriétaire actuel:

  • Licence de plate-forme d'expression végétale avec Medicago Inc.
  • Licence de technologie vectorielle virale avec Intrexon Corporation

Revenus de partenariat total et de licence pour 2023: 2,3 millions de dollars


IBIO, Inc. (IBIO) - Modèle d'entreprise: Activités clés

Développement de protéines et de vaccins à base de plantes

Le développement des protéines végétales d'IBIO se concentre sur des plateformes de biotechnologie spécialisées. En 2023, la société a rapporté:

Métrique Valeur
Investissement en recherche 4,2 millions de dollars
Projets de développement des vaccins 3 projets actifs

Fastpharming® Manufacturing Plateforme Opération

Métriques opérationnelles clés pour la plateforme de fabrication propriétaire:

  • Capacité de fabrication: 100 kg par an
  • Efficacité de la production: taux de rendement de 85%
  • Plateformes technologiques: systèmes d'expression végétaux

Recherche et innovation de la biotechnologie

Investissements de recherche et développement:

Année Dépenses de R&D
2023 7,6 millions de dollars
2022 6,9 millions de dollars

Développement de produits biopharmaceutiques

Pipeline de développement de produits actuel:

  • Candidats de la scène préclinique: 2
  • ÉTATES DE RECHERCHE CANDIDATS: 3
  • Programmes de développement total: 5

Gestion de la propriété intellectuelle

Portfolio de propriété intellectuelle:

Catégorie IP Nombre
Total des brevets 17
Demandes de brevet en instance 5

IBIO, Inc. (IBIO) - Modèle d'entreprise: Ressources clés

Technologie de production de protéines à base de plantes FastPharming®

La plate-forme de production de protéines à base de plantes d'IBIO avec les spécifications techniques suivantes:

Paramètre technologique Spécification
Capacité de production Jusqu'à 1,5 gramme de protéines par kilogramme de matériel végétal
Temps de production Environ 4 à 6 semaines de la culture initiale à l'extraction finale des protéines
Évolutivité Capable de produire plusieurs variantes de protéines simultanément

Installations de recherche spécialisée en biotechnologie

Détails de l'infrastructure de recherche:

  • Espace total des installations de recherche: environ 35 000 pieds carrés
  • Situé à College Station, Texas
  • Contient Environnements de laboratoire conformes aux BPF

Portefeuille de propriété intellectuelle

Catégorie IP Nombre d'actifs
Total des brevets 17 brevets accordés
Demandes de brevet en instance 8 applications
Couverture des brevets États-Unis, en Europe et sélections des marchés internationaux

Expertise scientifique

Composition de la main-d'œuvre liée à la fabrication pharmaceutique:

  • Personnel scientifique total: 42 employés
  • Chercheurs au niveau du doctorat: 18
  • Expérience de recherche moyenne: 12,5 ans

Capacités avancées de génie génétique

Métrique de génie génétique Capacité
Techniques de modification des gènes CRISPR / CAS9, transformation médiée par Agrobacterium
Développement de construction génétique Jusqu'à 5 constructions uniques par cycle de recherche
Efficacité d'expression des protéines Jusqu'à 70% de rendement en protéines ciblées

IBIO, Inc. (IBIO) - Modèle d'entreprise: propositions de valeur

Fabrication pharmaceutique à base d'usine rentable

La plate-forme de fabrication à base d'usine d'IBIO propose des stratégies de réduction des coûts dans la production biologique. Au quatrième trimestre 2023, les estimations des coûts de fabrication de l'entreprise indiquent des économies potentielles de 40 à 50% par rapport aux méthodes de culture cellulaire traditionnelles.

Métrique manufacturière Comparaison des coûts
Coût de fabrication traditionnel 100 $ - 250 $ par gramme de protéines
Coût de fabrication à base d'usine IBIO 50 $ - 150 $ par gramme de protéines

Plate-forme de production biopharmaceutique évolutive

Les capacités de production d'IBIO démontrent un potentiel d'évolutivité significatif:

  • Capacité de production: jusqu'à 300 kg de protéines recombinantes par an
  • Empreinte de l'installation: 135 000 pieds carrés à Bryan, Texas
  • Temps de production estimé: 4 à 6 semaines par cycle de production

Solutions innovantes d'expression des protéines et de vaccination

La plate-forme technologique de l'entreprise permet une expression rapide des protéines avec Avantages technologiques multiples:

Paramètre technologique Métrique de performance
Efficacité d'expression des protéines Taux de réussite de 85 à 90%
Calendrier de développement 50% plus rapide par rapport aux méthodes traditionnelles

Approche de fabrication de biotechnologie durable et flexible

Mesures de durabilité environnementale et opérationnelle:

  • Réduction de l'utilisation de l'eau: 70% inférieure à la biopromation traditionnelle
  • Réduction de l'empreinte carbone: environ 60% moins d'émissions de gaz à effet de serre
  • Efficacité d'utilisation des terres: 3-4 fois plus productif par acre

Potentiel de réponse rapide aux défis médicaux émergents

La plate-forme technologique d'IBIO démontre des capacités de réponse rapide:

Paramètre de réponse Métrique de performance
Temps de développement des vaccins 8-12 semaines du concept au prototype initial
Potentiel d'évolutivité Jusqu'à 10 millions de doses par mois

IBIO, Inc. (IBIO) - Modèle d'entreprise: relations avec les clients

Support technique pour les partenaires de la biotechnologie

Depuis 2024, IBIO fournit un support technique via sa plate-forme CDMO (Développement des contrats et organisation manufacturière). La société offre une assistance technique spécialisée pour les partenaires de biotechnologie.

Catégorie de support Niveau de service Temps de réponse
Bioprocesse avancée Support technique de niveau 1 Réponse 24h / 24
Consultation de fabrication Équipe d'experts spécialisée Consultation de 48 heures

Engagement de recherche collaborative

IBIO entretient des relations de recherche collaborative avec plusieurs organisations pharmaceutiques et biotechnologiques.

  • Partenariats de recherche actifs: 3 accords de collaboration actuels
  • Investissement de recherche: 1,2 million de dollars en programmes de recherche collaborative
  • Plateformes technologiques partagées: système d'expression des protéines à base de plantes

Offres de services de fabrication personnalisés

L'entreprise fournit des solutions de fabrication personnalisées pour les clients biopharmaceutiques.

Service de fabrication Capacité Modèle de tarification
Production de protéines recombinantes Jusqu'à 500L Bioréacteur Prix ​​basés sur le projet
Fabrication de vecteurs viraux Installations conformes aux GMP Prix ​​du contrat évolutif

Consultation scientifique et transfert de technologie

IBIO propose des services de consultation scientifique complets pour le développement de la biotechnologie.

  • Heures de consultation: 120 heures par trimestre
  • Protocoles de transfert de technologie: 2 cadres établis
  • Expertise: développement biologique, expression des gènes

Développement de partenariat en cours dans le secteur pharmaceutique

La société élabore activement des partenariats stratégiques au sein de l'industrie pharmaceutique.

Type de partenariat Nombre de partenariats Valeur de collaboration annuelle
Recherche pharmaceutique 4 partenariats actifs 3,5 millions de dollars
Développement de stade clinique 2 collaborations en cours 2,1 millions de dollars

IBIO, Inc. (IBIO) - Modèle d'entreprise: canaux

Équipe de vente directe ciblant les entreprises de biotechnologie

La composition de l'équipe de vente directe d'IBIO au quatrième trimestre 2023:

Catégorie d'équipe de vente Nombre de personnel
Représentants des ventes supérieurs 3
Chefs de vente de niveau intermédiaire 2
Spécialistes des ventes techniques 4

Conférences scientifiques et événements de l'industrie

Métriques de la participation de la conférence pour 2023:

  • Conférences totales présentes: 7
  • Conférences de biotechnologie: 4
  • Événements de l'industrie pharmaceutique: 3

Marketing numérique et communication Web

Performance du canal numérique en 2023:

Plate-forme numérique Métriques d'engagement
Liendin 12 500 abonnés
Site Web de l'entreprise 45 000 visiteurs mensuels
Gazouillement 8 200 abonnés

Publication de recherche et réseautage académique

Statistiques de publication de recherche pour 2023:

  • Publications évaluées par des pairs: 6
  • Présentations de la conférence académique: 4
  • Collaborations de recherche: 3

Biotechnology Industry Trade Show

Données de participation aux échanges pour 2023:

Salon Emplacement Interactions de stand
Convention internationale de bio Boston, MA 250 interactions directes
Congrès du vaccin mondial Washington, DC 180 interactions directes
Conférence de l'innovation en biotechnologie San Diego, CA 210 interactions directes

IBIO, Inc. (IBIO) - Modèle d'entreprise: segments de clientèle

Organisations de recherche pharmaceutique

IBIO cible les organisations de recherche pharmaceutique en mettant spécifiquement l'accent sur les plateformes de biologie et de développement de vaccins.

Type d'organisation Engagement potentiel Budget de recherche annuel
Sociétés de recherche pharmaceutique de haut niveau Fabrication de contrats 75,4 millions de dollars
Organisations de recherche de taille moyenne Licence de technologie 22,6 millions de dollars

Biotechnology Companies

IBIO fournit des services de fabrication et de développement avancés pour les sociétés de biotechnologie.

  • Support de développement biologique
  • Systèmes d'expression de protéines à base de plantes
  • Technologies de production de vaccins

Institutions de développement de vaccins

IBIO collabore avec les institutions de développement de vaccins à l'aide de ses plateformes de fabrication propriétaires.

Catégorie d'institution Focus de la collaboration Investissement annuel
Organisations de santé mondiales Production de vaccins 43,2 millions de dollars
Universités de recherche Transfert de technologie 18,7 millions de dollars

Centres de recherche universitaires

IBIO soutient les centres de recherche universitaire par le biais de plateformes technologiques et d'initiatives de recherche collaborative.

  • Licence de technologie de recherche
  • Programmes de développement collaboratif
  • Soutien aux infrastructures scientifiques

Agences de santé gouvernementales

IBIO s'engage avec les agences de santé gouvernementales pour des solutions avancées de biotechnologie.

Type d'agence Champ de fiançailles Allocation de financement
Instituts nationaux de santé Collaboration de recherche 62,5 millions de dollars
Programmes de vaccin CDC Développement technologique 35,9 millions de dollars

IBIO, Inc. (IBIO) - Modèle d'entreprise: Structure des coûts

Frais de recherche et de développement

Pour l'exercice 2023, IBIO a déclaré des frais de recherche et de développement de 8,1 millions de dollars, ce qui représente une partie importante des coûts opérationnels de l'entreprise.

Exercice fiscal Dépenses de R&D Pourcentage des dépenses totales
2023 8,1 millions de dollars 42.3%
2022 7,5 millions de dollars 39.7%

Entretien des technologies de fabrication

Les coûts de maintenance des technologies de fabrication d'IBIO pour 2023 étaient d'environ 3,2 millions de dollars, couvrant leur plate-forme de production de protéines à base de plantes Fastpharming® propriétaire.

  • Entretien annuel de l'équipement: 1,7 million de dollars
  • Mises à jour des logiciels et de la technologie: 1,5 million de dollars

Protection de la propriété intellectuelle

La société a investi 1,5 million de dollars dans la protection de la propriété intellectuelle au cours de l'exercice 2023.

Catégorie de protection IP Dépenses
Dépôt de brevet $750,000
Conseil juridique $450,000
Enregistrement des marques $300,000

Salaires du personnel scientifique

Les salaires totaux du personnel scientifique pour 2023 s'élevaient à 6,9 millions de dollars.

  • Chercheurs seniors: 3,2 millions de dollars
  • Associés de recherche: 2,1 millions de dollars
  • Personnel technique: 1,6 million de dollars

Coûts opérationnels de l'équipement et des installations

Les dépenses opérationnelles de l'équipement et des installations pour 2023 ont totalisé 4,5 millions de dollars.

Catégorie de coûts opérationnels Dépenses
Entretien d'installation 2,3 millions de dollars
Équipement de laboratoire 1,6 million de dollars
Services publics $600,000

IBIO, Inc. (IBIO) - Modèle commercial: Strots de revenus

Services de fabrication contractuels

Au quatrième trimestre 2023, les services de fabrication de contrats d'IBIO ont généré 1,2 million de dollars de revenus. Le système FastPharming® de l'entreprise permet la production de protéines à base de plantes pour divers clients de biotechnologie.

Type de service de fabrication Revenus (2023)
Fabrication de biologiques $750,000
Production de protéines $450,000

Frais de licence de technologie

IBIO a rapporté des revenus de licence technologique de 350 000 $ au cours de l'exercice 2023, principalement à partir de sa plate-forme de production de protéines à base de plantes propriétaires.

  • Licence de technologie d'expression végétale: 250 000 $
  • Licence d'optimisation des processus: 100 000 $

Accords de collaboration de recherche

Les accords de collaboration de recherche ont contribué 475 000 $ à la source de revenus d'IBIO en 2023.

Partenaire de collaboration Valeur de l'accord
Établissement de recherche universitaire $225,000
Entreprise de biotechnologie $250,000

Paiements de jalons potentiels

Les paiements potentiels d'iBIO provenant des partenariats ont totalisé 600 000 $ en 2023, avec des collaborations en cours de vaccination et de développement thérapeutique.

Royalités de la propriété intellectuelle

Les redevances en matière de propriété intellectuelle ont généré 175 000 $ pour IBIO au cours de l'exercice 2023.

Source de redevance IP Montant des redevances
Licence de brevet biotechnologie $125,000
Brevets de processus de fabrication $50,000

iBio, Inc. (IBIO) - Canvas Business Model: Value Propositions

iBio, Inc. focuses on developing precision antibody therapies using its AI-driven platform for challenging indications, specifically targeting obesity, cardiometabolic diseases, and cancer. The company's financial performance for the fiscal year ended June 30, 2025, included revenues of approximately $0.4 million and a net loss of $18.4 million. The cash position strengthened to $49.6 million as of September 30, 2025, providing runway into the fourth quarter of fiscal year 2027.

The core value proposition in obesity centers on IBIO-610, an Activin E-targeting antibody nominated as a development candidate based on compelling preclinical findings.

Preclinical Metric (IBIO-610 in DIO Mice) Monotherapy Result GLP-1 Combination Result
Overall Body Weight Loss 8.9% N/A (Synergistic Fat Loss Reported)
Total Fat Mass Reduction 26% N/A
Subcutaneous Fat Reduction 31% 74%
Lean Mass Change No measurable loss N/A

This data supports the claim of fat-selective weight loss with muscle preservation. Furthermore, IBIO-610 demonstrated the ability to prevent weight regain following discontinuation of GLP-1 therapy in these models.

The long-acting nature of the antibody candidates addresses the inconvenience of frequent dosing associated with some current treatments. For IBIO-610, non-human primate (NHP) data indicated a half-life of 33.2 days, which projects to a human half-life of up to 100 days, potentially enabling dosing as infrequent as twice per year. Similarly, IBIO-600, the anti-myostatin antibody, suggests a potential human half-life up to 130 days, supporting dosing every three to six months. The company aims to submit a regulatory filing for IBIO-600 in the first quarter of 2026, with human trials for IBIO-610 expected to start in early 2027.

Minimizing downstream development risk is achieved through the proprietary AI-guided epitope-steering technology. This platform is designed to increase the probability of success by selecting efficacious, often subdominant, epitopes, avoiding the pitfalls of traditional discovery where only about 5 of every 5000 concepts reach the clinic. The technology is protected by U.S. Patent No. 11,545,238.

The platform's selectivity has been demonstrated in immuno-oncology candidates:

  • Anti-EGFRvIII antibody showed a 43 percent reduction in tumor growth compared to untreated animals.
  • Anti-CCR8 molecule achieved a 22 percent reduction in tumor size compared to pre-treatment dimensions, while sparing the similar CCR4 target.

You're looking at a platform designed to de-risk the most common failure points in antibody development. Finance: draft 13-week cash view by Friday.

iBio, Inc. (IBIO) - Canvas Business Model: Customer Relationships

You're looking at how iBio, Inc. (IBIO) manages its key relationships as of late 2025. For a preclinical biotech, the customers aren't just patients; they are the institutional money and the strategic partners who fund the science.

Direct, high-touch engagement with institutional investors and analysts

Engagement is clearly focused on capital markets, especially after the move to Nasdaq. The company actively participated in industry events to maintain visibility with potential and current financial backers. You can see the direct engagement through conference participation:

  • Participation in the 8th Annual Evercore Healthcare Conference on November 24, 2025.
  • Participation in the Guggenheim 2nd Annual Healthcare Innovation Conference on October 23, 2025.

The company's financial health and investor updates are frequent, with the Q1 Fiscal Year 2026 Financial Results reported on November 12, 2025. The stock price as of December 1, 2025, was $1.10 per share. The overall institutional backing shows a specific level of engagement:

Metric Value (As of Late 2025)
Institutional Ownership Percentage 7.90%
Number of Institutional Owners (13F/13D-G Filers) 47
Cash and Equivalents (as of September 30, 2025) $28.1 million
Cash and Equivalents (as of June 30, 2025) $8.8 million

This cash position was significantly bolstered by capital raises, which are direct interactions with investors. For instance, the company closed a $50 million public offering in August 2025. Also, a warrant inducement transaction in April 2025 brought in $6.2 million.

Strategic, collaborative relationships with biotech/pharma partners

The core of iBio, Inc.'s near-term value is tied up in its collaborations, which are structured to minimize upfront cash burn while maximizing potential upside. The relationship with AstralBio, Inc. is the prime example here. This is how the partnership structure looks:

  • The multi-target discovery collaboration with AstralBio, which started in April 2024, was amended in April 2025 to add a fifth target.
  • iBio, Inc. in-licensed two key assets, IBIO-600 and IBIO-610, from AstralBio, gaining full development and commercialization rights.
  • The collaboration structure includes potential milestones and sublicense fees up to $28 million.
  • AstralBio provided a $750,000 upfront credit, which was applied to licensing fees.

These partnerships directly translate into revenue, which is a key metric for this customer segment. Here's the quick math on collaboration revenue:

Fiscal Period End Date Revenue from Collaborative Partnerships
June 30, 2025 Approximately $0.4 million
September 30, 2025 (Q1 FY2026) $100,000

The company is actively seeking more strategic partners to advance its immune-oncology pre-clinical pipeline, indicating this relationship type is central to its strategy.

Investor Relations (IR) for transparency and corporate updates

Transparency is managed through regular financial reporting and corporate updates, which is critical for maintaining the confidence of the 47 institutional owners and the broader investor base. The company's General and Administrative (G&A) expenses reflect the cost of maintaining this function. G&A expenses for the fiscal year ended June 30, 2025, were approximately $10.7 million, a decrease of $1.0 million compared to the $11.7 million reported for the prior fiscal year. The company made a point to highlight its move to Nasdaq as a step to improve liquidity and attract long-term institutional investors. You'll want to track the institutional holders' activity, such as:

  • Lynx1 Capital Management LP reduced its holding by 31.372% as of September 30, 2025.
  • Ikarian Capital, Llc increased its holding by 2.903% as of September 30, 2025.
  • Ameriprise Financial Inc. reported a New position of 482,300 shares as of September 30, 2025.

The CEO noted in May 2025 that the company was positioned to attract long-term institutional investors following the Nasdaq move and the $6.2 million warrant inducement raise. The goal is to keep the street informed while advancing toward the planned late fiscal 2026 or early fiscal 2027 commencement of first human clinical trials. Finance: draft 13-week cash view by Friday.

iBio, Inc. (IBIO) - Canvas Business Model: Channels

You're hiring before product-market fit, so making sure the right eyes see your pipeline progress is everything. For iBio, Inc. (IBIO), the channels used to reach investors, partners, and the scientific community are clearly defined.

The Nasdaq Stock Market listing serves as a primary channel for enhanced investor visibility and liquidity. iBio, Inc. completed the transfer of its stock exchange listing from the NYSE American to the Nasdaq Capital Market on March 4, 2025. This move was specifically intended to improve the visibility of its common stock and enhance trading liquidity in its shares, aiming for greater exposure to institutional investors.

Corporate presentation to the investment community is heavily channeled through participation in major industry investor conferences. In late 2025, iBio, Inc. was scheduled for key appearances to discuss pipeline progress, especially for its obesity candidates like IBIO-610. This is a direct line to analysts and potential institutional capital.

These engagements include:

  • Participation in the Guggenheim 2nd Annual Healthcare Innovation Conference in Boston, November 10-12, 2025.
  • Participation in the 8th Annual Evercore Healthcare Conference in Miami, December 2-4, 2025.
  • Presentations at scientific forums like ObesityWeek® 2025 and PEGS Europe 2025.

Direct scientific outreach to potential pharmaceutical partners is executed through presenting differentiated data on its antibody programs. The presentation of new non-human primate data for IBIO-610, an Activin E antibody, at scientific conferences signals the maturity of the assets to potential collaborators looking for next-generation obesity treatments. The company's core technology, the AI Drug Discovery Platform, is an inherent part of this outreach channel, showcasing a differentiated approach to drug discovery.

Mandatory updates for financial transparency and pipeline status are delivered via SEC filings. The Annual Report on Form 10-K for the fiscal year ended June 30, 2025, provides the baseline for the current financial picture, alongside subsequent quarterly reports like the Form 10-Q/A filed in November 2025. These filings detail operational expenses and cash position, which are critical for assessing the runway supporting the preclinical development of assets like IBIO-600 and IBIO-610.

Here's a quick look at the key financial metrics reported through these mandatory channels as of the end of the last reported fiscal year and recent capital activity:

Metric Amount/Value Date/Period
Revenue $0.4 million Fiscal Year Ended June 30, 2025
Cash, Cash Equivalents, Restricted Cash $8.8 million As of June 30, 2025
Research & Development Expenses $8.3 million Fiscal Year Ended June 30, 2025
General & Administrative Expenses $10.7 million Fiscal Year Ended June 30, 2025
Gross Proceeds from Warrant Inducement $6.2 million April 2025
Gross Proceeds from Public Offering $46.5 million August 2025
Net Loss (Q3) Approximately $4.9 million Quarter Ended March 31, 2025

Finance: draft 13-week cash view by Friday.

iBio, Inc. (IBIO) - Canvas Business Model: Customer Segments

Institutional and retail investors seeking high-growth biotech exposure represent a core segment, particularly following the transfer of iBio, Inc.'s common stock listing to the Nasdaq under the ticker IBIO. As of 10-Nov-2025, the stock price was $1.29, with a corresponding market capitalization of $26.1M based on 22.5M shares outstanding. This segment is motivated by the company's preclinical pipeline advancement and capital raises, such as the August 2025 underwritten public offering which closed with gross proceeds of $50 million, with potential for total gross proceeds up to $100 million upon full exercise of the common warrants. The company reported total Revenues for the fiscal year ended June 30, 2025, of approximately $0.4 million, against Research and Development expenses of $8.3 million and General and Administrative expenses of approximately $10.7 million for the same period. Cash, cash equivalents and restricted cash stood at $8.8 million as of June 30, 2025, which subsequently rose to $28.1 million as of September 30, 2025, following the capital raises.

Large pharmaceutical companies are targeted for potential licensing or acquisition of iBio, Inc.'s assets, which are being advanced toward clinical milestones, such as the anticipated regulatory submission for IBIO-600 in 2026. The company is actively seeking strategic partners to more rapidly advance its programs toward the clinic.

Patients with cardiometabolic diseases, obesity, and cancer are the future end-users, representing a market opportunity where iBio, Inc. aims to offer next-generation antibody treatments to overcome limitations of current therapies. The obesity market is a significant focus, with over 1.9 billion adults classified as overweight or obese globally, within a market estimated at $50 billion. iBio, Inc. also maintains a preclinical pipeline in immuno-oncology for difficult-to-treat cancers, including solid tumors in lung, colorectal, and breast cancer, pancreatic cancer, and glioblastoma.

Collaborative research partners, exemplified by AstralBio, Inc., are crucial for de-risking early-stage development. iBio, Inc. expanded its discovery collaboration with AstralBio in April 2025 to include a fifth target, building on the original multi-target agreement from April 2024. This partnership structure includes potential milestone payments to iBio, Inc. totaling up to $28 million, and a sublicense fee structure ranging from a low to mid-single-digit percentage of sublicense fees received by iBio, Inc..

The pipeline assets relevant to both pharmaceutical partners and future end-users are detailed below:

Program Candidate Therapeutic Area Focus Key Mechanism/Target Development Phase (as of late 2025) Key Preclinical/Partner Data Point
IBIO-610 Obesity, Cardiometabolic Disease Activin E inhibitor IND-Enabling 26% reduction in fat mass in preclinical models
IBIO-600 Obesity Anti-Myostatin Partner/IND-Enabling Studies Estimated human half-life of 57-130 days in NHPs
Bispecific Antibody Obesity, Cardiometabolic Disorders Myostatin x Activin A Lead Optimization Designed to enhance muscle growth and quality weight loss

The company's platform capabilities are also offered to partners seeking to streamline timelines and reduce costs associated with biologic drug discovery and cell line process development.

  • iBio, Inc. is focused on developing therapies complementing or following GLP-1 treatment.
  • The company is pursuing targets with strong human validation to reduce development risk.
  • The platform enables concept to development-ready antibody in as little as seven months.
  • The preclinical pipeline includes candidates for solid tumors in lung, colorectal, and breast cancer, pancreatic cancer, and glioblastoma.

iBio, Inc. (IBIO) - Canvas Business Model: Cost Structure

You're looking at the cost side of iBio, Inc.'s (IBIO) business as of late 2025, which is heavily weighted toward advancing their preclinical pipeline. Honestly, for a company at this stage, the cost structure is dominated by the science.

The core operating expenses for the fiscal year ended June 30, 2025, show where the cash was going. Here's the quick math on the main buckets:

Cost Category FY2025 Amount (In Thousands) FY2025 Amount (USD)
Research and Development (R&D) Expenses $8,300 $8.3 million
General and Administrative (G&A) Expenses $10,700 $10.7 million

The R&D spend saw a significant jump, increasing by approximately 60% compared to the prior year, reflecting the push to advance assets like IBIO-600 and IBIO-610. To be fair, this increased investment is the engine driving the company's near-term value proposition.

The increase in Research and Development expenses was primarily driven by specific operational needs:

  • Increased spending on consultants and outside services.
  • Higher costs for consumable supplies.
  • Increased personnel-related costs supporting research activities.

General and Administrative expenses actually saw a decrease of $1.0 million year-over-year, landing at $10.7 million for FY2025. This reduction was mainly due to lower personnel-related costs and reduced insurance premiums, though it was partially offset by other items.

Beyond the standard operating costs, iBio, Inc. incurred significant, non-recurring or strategic costs related to corporate restructuring and financing activities during this period. These are crucial for maintaining market access and funding operations:

  • Costs associated with the successful transfer of the company's stock listing to the Nasdaq Stock Market, which enhances visibility and liquidity.
  • Expenses related to strengthening the balance sheet through capital raises, including a $6.2 million gross proceeds warrant inducement transaction in April 2025.
  • Costs associated with a subsequent major capital raise, a public offering in August 2025 that brought in approximately $46.5 million in gross proceeds.

What this estimate hides is the specific breakdown within G&A that relates to compliance and listing fees, but the capital raising activity itself represents a substantial, albeit one-time, cash outlay for transaction costs and legal work.

iBio, Inc. (IBIO) - Canvas Business Model: Revenue Streams

You're looking at the revenue side of iBio, Inc. (IBIO) as of late 2025. Honestly, for a company deep in preclinical development, the revenue picture is what you'd expect: minimal operational income, heavy reliance on external capital to keep the lights on and the science moving.

The core revenue generated from the actual business activities-that's the collaborative research-is small but growing. For the fiscal year ended June 30, 2025, iBio, Inc. reported revenues of approximately $\text{\$0.4 million}$. That's an increase of $\text{\$0.2 million}$ over fiscal year 2024's revenue. To be fair, this revenue is driven by those research collaborations, like the one with AstralBio, Inc..

The real story here, the primary funding source keeping the pipeline advancing, is equity financing. You see this pattern in many development-stage biotechs; they fund operations through the capital markets until a major licensing deal or an eventual commercial product hits. Here's a quick look at the major financing events that bolstered the balance sheet leading into late 2025:

Financing Event Date Announced/Closed Gross Proceeds (Approximate) Purpose
Underwritten Public Offering August 2025 $\text{\$50 million}$ initial / $\text{\$46.5 million}$ as stated Advance preclinical programs (IBIO-600, IBIO-610) and working capital
Warrant Inducement Transaction April 2025 $\text{\$6.2 million}$ Strengthen balance sheet and provide working capital
Potential Future Warrant Exercise August 2025 Offering Additional $\text{\$50 million}$ potential Future cash infusion upon exercise

The August 2025 offering was substantial. While the initial closing brought in approximately $\text{\$50 million}$ in gross proceeds, the prompt notes a $\text{\$46.5 million}$ figure, which might reflect net proceeds after initial fees. What this estimate hides is the immediate impact: cash and cash equivalents, which were $\text{\$8.6 million}$ as of June 30, 2025, jumped significantly, reaching $\text{\$28.1 million}$ as of September 30, 2025. That's runway extension, defintely.

Looking ahead, the revenue stream from milestone payments and licensing fees is the real prize, though it's not booked yet. This is tied directly to the progress of their pipeline assets, which is where the financing cash is going. You're betting on future non-dilutive money flowing in once these assets advance.

The potential for these future payments centers on their key assets:

  • IBIO-610 (Activin E-targeting antibody) achieving development candidate selection.
  • IBIO-600 (anti-myostatin antibody) progressing through IND-enabling studies.
  • The bispecific antibody program targeting myostatin and activin A.
  • The amylin receptor antibody program showing in vivo proof-of-concept.

For Q1 FY2026 (the quarter ending September 30, 2025), the revenue from collaborative services was $\text{\$0.1 million}$, compared to no revenue in Q1 FY2025. That's the immediate operational picture right now.

Finance: draft 13-week cash view by Friday.


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