Syneron Bio
Both parties publicly confirmed the AstraZeneca collaboration. A 2026 financing announcement states that proceeds will advance the pipeline into clinical development; specific human oral PK data were not disclosed.
All cataloged matching companies in this field are shown below. Expand filters to narrow the results.
Disease tags identify mentions in recorded facts or pipeline text, not approved indications or a complete pipeline. Platform service providers may have no disease-specific tag.
79 matching companies
Both parties publicly confirmed the AstraZeneca collaboration. A 2026 financing announcement states that proceeds will advance the pipeline into clinical development; specific human oral PK data were not disclosed.
The company website confirms the Macoral® / Simgut® platform and collaboration with BrightGene. The pipeline image reviewed is historical; current clinical stages require confirmation.
FDA approved ICOTYDE for plaque psoriasis on 2026-03-17. Its prescribing information reports human exposure and food effects.
A U.S. commercial benchmark for oral octreotide, with label evidence for enteric capsule composition and a substantial food effect. Its EU authorization has been withdrawn.
AUBE00 is an oral macrocyclic peptide in Phase 1. LUNA18 was discontinued in 2025; the company report confirms oral absorption in humans.
LUPKYNIS is a U.S.-approved oral treatment for lupus nephritis. Its capsule label discloses lipid and surfactant ingredients.
The discovery and collaboration partner for ICOTYDE. Its website also lists PN-881 (oral IL-17A/F) and other early oral programs; the company is recorded separately from J&J.
CID-078, from the MXMO macrocycle platform, is an oral cyclin A/B RxL inhibitor in Phase 1; CID-165 targets cyclin D1.
Iterative design, synthesis, and experimental optimization improve synthetic macrocyclic peptide potency, selectivity, and permeability. The company collaborates with argenx on oral macrocycle programs.
The website explicitly focuses on cell-permeable, orally available cyclic peptides using machine learning, automated design, synthesis, and testing. No named clinical candidates were disclosed.
Uses AI to design macrocycles de novo. The website lists oral / cell-permeable approaches and an α4β7 IBD program; website percentages are not converted into clinical-stage assignments.
Uses AI, physics-based simulation, peptide chemistry, and oral formulation development for oral immunology and cardiometabolic peptides; operates in Shanghai and Pennsylvania.
nGen combines AI and automated synthesis to optimize oral properties of nCycles and has a multi-target cardiometabolic collaboration with Novo. The company describes nCycles as fully synthetic macrocyclic NCEs.
The PDPS-derived oral peptide pipeline includes a myostatin program listed as IND-enabling, plus other oral candidates; it is recorded separately from the radiopharmaceutical peptide pipeline.
HS-20118 / AVR-001 is an oral IL-23R cyclic peptide with disclosed Phase 1 human data. Rights outside Greater China were licensed to Avere.
AVR-001 is Hansoh's HS-20118, with an exclusive license outside Greater China. A 2026 announcement proposed a merger with NextCure; the transaction is not recorded as closed.
HSK47388 is an oral IL-23 inhibitory peptide in Phase 2 for psoriasis. Relative exposure data support its enhancer formulation, while cyclization and absolute oral bioavailability remain unconfirmed.
SAL0167 is an internally developed cyclic peptide program for hyperlipidemia that received NMPA clinical trial authorization in 2026. Authorization is not treated as evidence of actual dosing.
The website lists oral cyclic peptides NGA-101 (IL-4Rα), NGA-102 (TL1A), and NGA-103 (TSLP). Pipeline stage graphics cannot be verified through text extraction alone.
The MO-PION oral macromolecule platform website explicitly lists semaglutide, heparin, and micafungin applications. Micafungin provides a lead for cyclic peptide applications.
The website explicitly identifies an ORALINK oral α4β7 cyclic peptide co-development program with D&D at lead optimization, recorded separately from radiopharmaceutical / conjugate programs.
ORALINK combines ligand conjugation, lipidation, and excipient strategies. The α4β7 cyclic peptide program with QIC is in lead optimization; its GLP-1 human evidence does not transfer to cyclic peptides.
Signed a next-generation oral peptide co-development agreement with D&D explicitly including macrocyclic peptides. Its role is AI design; independent ownership of a disclosed clinical drug has not been established.
The company disclosed a patent for an oral semaglutide nanoparticle formulation. This is a noncyclic peptide delivery reference, not clinical validation for cyclic peptides.
The website separately describes H1K, an oral anti-obesity candidate, and ESAIDD cyclic peptide discovery. This review could not confirm that H1K is cyclic or has human results.
Co-commercializes approved LINZESS and holds regional rights, alongside oral peptide discovery through Nimble. ABBV-859 is in Phase 1; its exact structure and mapping to Nimble assets remain unconfirmed.
On 2026-10-22, the company announced a proposed acquisition of PepStar's HCXT-2001 oral macrocyclic peptide program. Its Q3 announcement confirms Phase 1; closing conditions remain outstanding.
Counterparty for the HCXT-2001 transaction. Its role is recorded separately from Gilead's; the shared candidate is not counted as two independent drugs. The relationship between the Chinese sponsor and English legal entity requires confirmation.
Uses AI to design oral IL-17A/F inhibitors. The company describes fully synthetic, compact cyclic peptidomimetics containing nonnatural amino acids.
A September 2026 company announcement states that an unnamed MSD candidate using its oral technology entered Phase 1. The candidate structure is not disclosed, so it cannot be classified as a cyclic peptide.
Soteria provides protective excipients, Phloral provides targeted release, and UTAC provides active transport of macromolecules. Cyclic peptide applications require separate validation.
The Novo collaboration uses gastrointestinal tissue screening and formulation platforms to develop oral biologics. Specific drugs and cyclic peptide structures have not been disclosed.
Peptelligence previously conducted feasibility studies with Ferring to convert injectable peptides into oral formulations. It is retained as a historical delivery approach; current operations and ownership require verification.
EB613 is oral PTH(1-34), with disclosed clinical results and new-formulation bridging data and a planned Phase 3 program. Human evidence for this linear peptide is used only as a platform reference.
RaniPill is a swallowable robotic capsule. RT-101 octreotide is a historical human development program whose current activity is unconfirmed, recorded separately from conventional intestinal permeation enhancement.
NEORAL cyclosporine is a classic benchmark for oral cyclic peptides and microemulsion preconcentrates; it should not be assumed bioequivalent to Sandimmune.
LINZESS (linaclotide) is an oral peptide with multiple disulfide bonds and a GC-C agonist acting locally in the gastrointestinal tract. Systemic bioavailability is not the primary success criterion.
TRULANCE (plecanatide) is an oral disulfide-constrained peptide and GC-C agonist acting locally in the gastrointestinal tract. Regional status is based on the Canadian product monograph reviewed.
Swallowed DDAVP desmopressin tablets are a classic oral disulfide peptide reference. Swallowed, orally disintegrating, and sublingual products should be recorded separately.
Collaborates with Biogen to discover and optimize oral macrocyclic peptides for immune diseases. Named targets, candidates, and human results have not been disclosed.
Industry partner for Dayra's oral macrocyclic peptide collaboration, responsible for subsequent development and potential commercialization. Its role is recorded separately from Dayra's using a shared program identifier.
Conducts multi-target oral macrocyclic peptide research with Unnatural Products. Evidence supporting marketed antibody products does not raise the evidence grade of the macrocycle program.
Entered chronic-disease macrocyclic peptide research through the Syneron Bio collaboration. No named clinical oral candidate from that collaboration has been disclosed.
Works with Orbis on oral macrocycle discovery and with Vivtex on delivery. Success with oral semaglutide does not automatically validate the collaborative macrocycle program.
SG6001 is an oral PCSK9 cyclic peptide. Official materials confirm a preclinical program and an out-licensing strategy; clinical status of other antifungal candidates is not applied to this program.
PL8177 is a colon-delivered cyclic heptapeptide MC1R agonist. The company reported Phase 2 UC proof of concept and explicitly welcomes partnerships / licensing.
Alisporivir (Debio 025) is a cyclosporine-derived cyclophilin inhibitor with historical clinical development. A 2021 trial does not establish current active status.
PepiX™ connects AI, automated synthesis, and experimental screening. The website identifies oral cyclic peptides as a priority; food-peptide GRAS status is not pharmaceutical evidence.
The company's interim report describes peptidomimetic macrocycle discovery, optimization, and oral applications. DEL and platform capabilities do not establish human oral evidence for proprietary candidates.
Provides optimization of macrocyclic peptides derived from mRNA / phage display. Its website reports involvement in developing Merck's oral PCSK9 peptide MK-0616.
Microcycle® functionally screens compact macrocycles in live cells and develops macrocycle-derived drugs. This review did not confirm a named oral cyclic peptide candidate.
Its peptide screening platform covers linear, cyclic, and helical structures, so it is included as an adjacent discovery capability. It is not automatically classified as a validated oral cyclic peptide drug developer.
T25 is an oral octreotide acetate tablet. MED&SSE produces its shell and drug-containing core; FDA IND clearance was disclosed in 2026.
Original company materials confirm cyclic peptides as a development modality. This review did not find a primary announcement sufficient to verify a specific oral candidate and its current stage.
An investor record describes program 629 as an oral IL-23 cyclic peptide with PK suggesting once-weekly potential. Human results and the latest stage were not confirmed in this review.
The OralVantage™ oral peptide platform combines molecular stabilization and formulation strategies. It is included as a noncyclic peptide platform reference; validated oral cyclic peptides are not assumed.
Founded in 2026, this early-stage oral long-acting peptide company describes molecular design, microbial expression, and OMV packaging / delivery. Cyclic peptide identity and human evidence require verification.
An important adjacent company in bicyclic peptide screening and conjugation. Its disclosed nonoral clinical pipeline is not evidence of oral cyclic peptide success.
Rencofilstat (CRV431) has oral clinical studies in MASH. Hepion transferred related assets to Panetta in 2025; the record preserves the historical development and change in rights.
ST-0529 is an oral cyclosporine formulation for UC with historical Phase 2 registration. The Romanian record reviewed is marked prematurely ended. Current ownership and company status require verification.
SOR102 is a locally acting oral TNF / IL-23 bispecific single-domain antibody with a primary Phase 1 study. It is included as a noncyclic oral biologic reference.
The ST-0529 oral cyclosporine Phase 2 registry lists the company as a study supporter. That regional record ended prematurely; current development rights or collaboration budgets are not inferred.
LIPFENDRA is a U.S.-approved oral PCSK9 inhibitor. Its label confirms sodium caprate and approximately 1% oral bioavailability.
Provides process development, analytical services, and GMP clinical manufacturing for cyclic peptides, stapled peptides, and peptidomimetics. Classified as a manufacturing service provider; client drugs are not treated as proprietary pipelines.
The website describes a client case for a non-GLP-1 oral cyclic peptide, from library synthesis and lead optimization through GMP preparation. Only service capability is recorded; the unnamed client is neither identified nor guessed.
CLIPS™ supports monocyclic, bicyclic, and tricyclic constrained peptides, screening, and optimization. Recorded at the integrated-group level; oral suitability requires program-level validation.
The company describes constrained peptide chemistry involving disulfides, lactam bridges, stapling, and other cyclization approaches. This review did not confirm a proprietary oral cyclic peptide candidate.
MAUD 1.0 combines generative AI, physics-based modeling, and quantum simulations to design cyclic peptides. The company explicitly optimizes oral bioavailability and cell permeability and works with pharmaceutical partners on discovery.
An October 2026 research collaboration and exclusive option agreement with Generian advances an oral macrocyclic peptide FcRn antagonist. This research-stage program is separate from Processa’s Phase 2 small-molecule BTK inhibitor VT-7208.
A company emerging from the UPMC/University of Pittsburgh ecosystem, Generian entered an October 2026 research collaboration and exclusive option arrangement with Processa for an oral macrocyclic peptide FcRn antagonist.
A cyclic peptide discovery company using trillion-scale peptide libraries, screening, and chemical optimization for internal programs and partnerships. Its website identifies oral peptide therapeutics as one potential application.
Offers integrated structural biology, AI design, cyclic peptide synthesis, DMPK, and process-development capabilities. A September 2026 company article discusses oral cyclic peptide bioavailability, impurity control, and scale-up.
Holds exclusive development, manufacturing, and commercialization rights for linaclotide in Japan. It is included as a regional partner for an approved, locally acting oral disulfide-constrained peptide.
Ironwood’s Q2 2026 filing confirms that Grand Life Sciences assumed AstraZeneca’s linaclotide development, manufacturing, and commercialization rights in China, including Hong Kong and Macau, in May 2026.
Aurinia’s Q3 2026 filing identifies Otsuka as the development and commercialization partner for oral voclosporin in Japan, the EU, the UK, and other specified territories, supported by a commercial supply arrangement.
Provides cyclic and other complex peptide synthesis, noncanonical amino-acid modifications, peptide libraries, and in vitro oral-bioavailability screening. It is included as a discovery and development service provider.
Original technical materials describe macrocycle, stapled peptide, and bicyclic peptide synthesis. Included as discovery / manufacturing services, not elevated to an oral clinical drug developer.
An original October 2026 investor record identifies oral cyclic peptides as a priority business and states that orders have been received. Only manufacturing services are recorded; proprietary drug pipelines are not inferred.
The TIDES platform covers process development, analytics, and manufacturing for monocyclic, polycyclic, and modified peptides. This review did not confirm a named oral cyclic peptide program.
Coverage expands from sourced records; this database does not claim all biopharma companies.