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Climb Bio to Present on CLYM116 and Budoprutug Programs at European Renal Association (ERA) Congress 2026

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Climb Bio (Nasdaq: CLYM) will present new data on its CLYM116 and budoprutug programs at the European Renal Association (ERA) Congress 2026 in Glasgow, June 3-6, 2026.

Presentations cover PK/PD modeling and initial Phase 1 safety data for CLYM116 in IgA nephropathy and a Phase 2 trial-in-progress poster for budoprutug in primary membranous nephropathy.

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News Market Reaction – CLYM

+3.55%
9 alerts
+3.55% Session close to close
+6.6% Peak in 26 hr 41 min
$698.50M Market Cap
0.4x Rel. Volume

In the May 26 session, CLYM gained 3.55%, reflecting a moderate positive market reaction. Argus tracked a peak move of +6.6% during that session. Our momentum scanner triggered 9 alerts that day, indicating moderate trading interest and price volatility.

Data tracked by StockTitan Argus on the day of publication.

Market Context

This announcement highlights upcoming ERA 2026 presentations for CLYM116 in IgA nephropathy and the ...
Analysis

This announcement highlights upcoming ERA 2026 presentations for CLYM116 in IgA nephropathy and the Phase 2 PrisMN study of budoprutug in primary membranous nephropathy, reinforcing Climb Bio’s dual-program focus. Recent history shows significant R&D progress, expanded clinical activity, and fresh capital from a $110.0 million private placement. Investors may watch for detailed safety and PK/PD data, as well as future readouts across pMN, ITP, and SLE mentioned in prior filings and updates.

Key Figures

ERA 2026 dates: June 3–6, 2026 CLYM116 study phase: Phase 1 Budoprutug study phase: Phase 2 +5 more
8 metrics
ERA 2026 dates June 3–6, 2026 European Renal Association Congress schedule
CLYM116 study phase Phase 1 Ongoing study in healthy volunteers
Budoprutug study phase Phase 2 PrisMN trial in primary membranous nephropathy
Focused oral abstract 780 CLYM116 focused oral presentation abstract number
Poster abstract 655 PrisMN budoprutug poster abstract number
Focused oral time 15:03–15:09 BST CLYM116 session on June 5, 2026
Poster session dates June 4–5, 2026 PrisMN poster at ERA 2026
Poster session hours 08:15–18:15 BST PrisMN poster viewing window

Historical Context

5 past events · Latest: May 14 (Positive)
Pattern 5 events
Date Event Sentiment 24h Move Catalyst
May 14 Clinical data preview Positive -0.7% Announced new budoprutug clinical data presentation at EHA 2026.
May 12 Investor conferences Neutral +0.5% Planned participation in two upcoming investor conferences with webcasts.
May 7 Earnings and updates Neutral -2.5% Reported Q1 2026 results, program updates, and noted $110M private placement.
May 5 R&D spotlight Positive +18.2% Topline SC budoprutug data and Fast Track designation with multiple 2026 readouts.
Apr 28 Private placement Negative -2.5% Announced $110.0M equity financing via common shares and pre-funded warrants.

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

Pattern Detected

Positive R&D and designation updates have previously coincided with strong upside, while financing and data-presentation headlines often saw mild or negative moves.

Recent Company History

Recent news shows Climb Bio advancing budoprutug and CLYM116 alongside balance-sheet strengthening. An April 28 private placement of $110.0 million was followed by an 18.16% move after a budoprutug R&D spotlight on May 5 highlighting Fast Track status and robust B-cell depletion. Subsequent Q1 results on May 7 and conference/data-presentation updates on May 12 and May 14 had modest price impacts. Today’s ERA 2026 presentation update continues this pattern of clinical and conference-driven visibility for both lead programs.

Key Terms

pharmacokinetic/pharmacodynamic, nonhuman primates, monoclonal antibody, iga nephropathy, +3 more
7 terms
pharmacokinetic/pharmacodynamic medical
"Climb Bio will present pharmacokinetic/pharmacodynamic modeling from nonhuman primates"
Pharmacokinetic/pharmacodynamic (PK/PD) describes two linked ideas: pharmacokinetics is how a drug moves through the body (how fast it’s absorbed, spread, broken down and eliminated) and pharmacodynamics is how the drug affects the body (the relationship between dose and response). Investors care because strong, predictable PK/PD data reduce uncertainty about effective dosing, safety and likelihood of regulatory approval—similar to knowing a car’s fuel efficiency and braking before buying, which lowers the risk of a costly surprise.
nonhuman primates medical
"modeling from nonhuman primates to humans for CLYM116, a novel ‘sweeper’"
Nonhuman primates are members of the primate family—such as monkeys and apes—used in biomedical research because their biology and immune systems are closer to humans than other animals. For investors, they matter because studies in these animals often shape safety and effectiveness data required by regulators, affecting drug development timelines, costs, supply constraints, and public or regulatory scrutiny much like a crucial early road test that can determine whether a medicine moves forward to human trials.
monoclonal antibody medical
"CLYM116, a novel ‘sweeper’ anti-APRIL monoclonal antibody, which is being developed"
A monoclonal antibody is a laboratory-made protein designed to recognize and attach to a specific target in the body, such as a disease-causing substance or cell. It functions like a highly precise lock-and-key tool, helping to treat or detect illnesses. For investors, companies developing monoclonal antibodies can represent promising opportunities in the healthcare sector, especially as these treatments often address unmet medical needs.
iga nephropathy medical
"monoclonal antibody, which is being developed to treat IgA nephropathy (IgAN)."
A kidney disease caused when deposits of the antibody called IgA collect in the tiny filters of the kidney, gradually reducing their ability to clear waste — like grit building up in a water filter. It matters to investors because it creates demand for diagnostics, drugs and long‑term care, drives clinical trial activity and regulatory decisions, and can influence the financial outlook of companies in pharma, biotech, medical devices and health insurance.
igan medical
"monoclonal antibody, which is being developed to treat IgA nephropathy (IgAN)."
IgAN, short for IgA nephropathy, is a chronic kidney disease in which an immune protein called IgA builds up in the kidneys, slowly damaging the filters that remove waste from the blood. Think of it as rust accumulating in a water filter: over time the filter clogs and performance declines. It matters to investors because it is a leading cause of kidney failure with large unmet treatment needs, driving clinical development, regulatory milestones, and potential market opportunity for new therapies.
primary membranous nephropathy medical
"Phase 2 study of budoprutug, a novel anti-CD19 monoclonal antibody, in primary membranous nephropathy"
An autoimmune kidney disorder in which the immune system attacks the thin filtering layer of the kidney, causing protein to leak into the urine and, over time, reduced kidney function—imagine tiny coffee filters developing holes and letting grounds through. It matters to investors because it shapes demand for diagnostics and therapies, drives clinical trials and regulatory decisions, and can influence drug revenues, treatment costs and insurer exposure tied to chronic kidney disease outcomes.
phase 2 medical
"PrisMN, its ongoing Phase 2 study of budoprutug, a novel anti-CD19"
Phase 2 is the mid-stage clinical trial where a new drug or treatment is tested in a larger group of patients to see if it works and to keep checking safety after initial human testing. Think of it as a field test that proves whether a product actually delivers its promised benefit. Investors watch Phase 2 closely because its results strongly influence a medicine’s chances of reaching the market, the size of its potential sales, and the company’s valuation.

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

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WELLESLEY HILLS, Mass., May 26, 2026 (GLOBE NEWSWIRE) -- Climb Bio, Inc. (Nasdaq: CLYM), a clinical stage biotechnology company developing therapeutics for patients with immune-mediated diseases, today announced upcoming presentations for its CLYM116 and budoprutug programs at the European Renal Association Congress 2026, which will be held in Glasgow, Scotland June 3-6, 2026.

Climb Bio will present pharmacokinetic/pharmacodynamic modeling from nonhuman primates to humans for CLYM116, a novel ‘sweeper’ anti-APRIL monoclonal antibody, which is being developed to treat IgA nephropathy (IgAN). Initial safety data from the ongoing CLYM116 Phase 1 study in healthy volunteers will also be presented.

The Company will also present a trial-in-progress poster for PrisMN, its ongoing Phase 2 study of budoprutug, a novel anti-CD19 monoclonal antibody, in primary membranous nephropathy (pMN).

Abstracts are available on the ERA 2026 website here.

Focused Oral Details

Title: CLYM116, a Novel ‘Sweeper’ Anti-APRIL mAb: Extrapolation of PK and Ig Suppression from NHPs to Healthy Volunteers and Initial Phase 1 Data
Session Topic: Glomerular & tubulo-interstitial diseases
Abstract Number: 780
Date / Time: June 5, 2026, 15:03-15:09 BST
Location: Focused Oral Room 2

Poster Details

Title: PrisMN: Phase 2 Study to Evaluate the Safety and Efficacy of Budoprutug, a Low-Fucosylated Anti-CD19 mAb, in Primary Membranous Nephropathy
Session Topic: Glomerular & tubulo-interstitial diseases
Abstract Number: 655
Date / Time: June 4-5, 2026, from 08:15-18:15 BST
Location: Research Zone: Hall 4 (Ground Floor)

About Climb Bio, Inc.
Climb Bio, Inc. is a clinical-stage biotechnology company with a mission to deliver high impact, disease-modifying medicines for individuals living with immune-mediated diseases, including those affecting kidney health. The Company’s pipeline includes, budoprutug, an anti-CD19 monoclonal antibody that has potential to treat a broad range of B-cell mediated diseases, and CLYM116, an anti-APRIL monoclonal antibody being developed for IgA nephropathy. For more information, please visit climbbio.com

About Budoprutug
Budoprutug is a clinical-stage, anti-CD19 monoclonal antibody with the potential to address a broad range of B-cell mediated, immune-driven diseases. Designed with enhanced effector function and low picomolar affinity, budoprutug targets and depletes CD19-expressing B cells, including plasmablasts and certain plasma cells, key sources of pathogenic autoantibodies. Early clinical data suggest budoprutug may offer durable B-cell depletion, rapid reductions in autoantibodies, and clinical remission in primary membranous nephropathy (pMN). Budoprutug is being evaluated in clinical trials for pMN, immune thrombocytopenia (ITP), and systemic lupus erythematosus (SLE). A subcutaneous formulation is also in development to enable broader patient access. Budoprutug has been granted Orphan Drug Designation and Fast Track Designation by the FDA for the treatment of pMN.

About CLYM116
CLYM116 is a clinical-stage monoclonal antibody targeting APRIL (A Proliferation-Inducing Ligand), a key driver of pathogenic B-cell activity in autoimmune diseases. CLYM116 employs a novel pH-dependent bind-and-release ‘sweeper’ mechanism to potently block APRIL signaling, promote lysosomal degradation of APRIL, and recycle the antibody to extend its half-life. This differentiated design offers the potential for rapid, deep, and durable inhibition of APRIL with a favorable safety profile and less frequent dosing. CLYM116 is being advanced for the treatment of IgA nephropathy (IgAN) and may also have broader utility across other B-cell mediated diseases where APRIL plays a critical role.

Forward-Looking Statements
This press release contains “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995, including without limitation statements regarding: future expectations, plans and prospects for Climb Bio; expectations regarding the therapeutic benefits, clinical potential and clinical development of budoprutug and CLYM116; the anticipated timelines for announcing data from Climb Bio’s ongoing and planned clinical trials; the anticipated benefits of Climb Bio’s technology transfer and exclusive license agreement with Mabworks; plans for the development strategy for budoprutug and CLYM116; potential commercial opportunity for budoprutug in primary membranous nephropathy; potential commercial opportunity for CLYM116 in IgA nephropathy; the sufficiency of Climb Bio’s cash resources for the period anticipated; and other statements containing the words “anticipate,” “believe,” “continue,” “could,” “estimate,” “expect,” “intend,” “may,” “plan,” “potential,” “predict,” “project,” “should,” “suggest,” “target,” “would,” “will,” “working” and similar expressions. Forward-looking statements are based on management’s current expectations of future events and are subject to a number of risks and uncertainties that could cause actual results to differ materially and adversely from those set forth in, or implied by, such forward-looking statements. Climb Bio may not actually achieve the plans, intentions or expectations disclosed in these forward-looking statements, and you should not place undue reliance on these forward-looking statements. These risks and uncertainties include, but are not limited to, important risks and uncertainties associated with: the ability of Climb Bio to timely and successfully achieve or recognize the anticipated benefits of its acquisition of Tenet Medicines, Inc. and its technology transfer and exclusive license agreement with Mabworks; Climb Bio’s ability to advance budoprutug and CLYM116 on the timelines expected or at all and to obtain and maintain necessary approvals from the U.S. Food and Drug Administration and other regulatory authorities; obtaining and maintaining the necessary approvals from investigational review boards at clinical trial sites and independent data safety monitoring boards; replicating in clinical trials positive results found in early-stage clinical trials or nonclinical studies; competing successfully with other companies that are seeking to develop treatments for primary membranous nephropathy, immune thrombocytopenia, systemic lupus erythematosus, IgA nephropathy and other immune-mediated diseases; maintaining or protecting intellectual property rights related to budoprutug, CLYM116 and/or its other product candidates; managing expenses; changes in applicable laws or regulation; the possibility that Climb Bio may be adversely affected by other economic, business and/or competitive factors; and raising the substantial additional capital needed, on the timeline necessary, to continue development of budoprutug, CLYM116 and any other product candidates Climb Bio may develop. For a discussion of other risks and uncertainties, and other important factors, any of which could cause Climb Bio’s actual results to differ materially from those contained in the forward-looking statements, see the “Risk Factors” section, as well as discussions of potential risks, uncertainties and other important factors, in Climb Bio’s most recent filings with the U.S. Securities and Exchange Commission. In addition, the forward-looking statements included in this press release represent Climb Bio’s views as of the date hereof and should not be relied upon as representing Climb Bio’s views as of any date subsequent to the date hereof. Climb Bio anticipates that subsequent events and developments will cause Climb Bio’s views to change. However, while Climb Bio may elect to update these forward-looking statements at some point in the future, Climb Bio specifically disclaims any obligation to do so, except as required by law.

Investors and Media
Carlo Tanzi, Ph.D.
Kendall Investor Relations
ctanzi@kendallir.com


FAQ

What will Climb Bio (NASDAQ: CLYM) present at ERA Congress 2026?

Climb Bio will present data on its CLYM116 and budoprutug programs at ERA Congress 2026. According to the company, sessions include PK/PD modeling and initial Phase 1 safety data for CLYM116, plus a trial-in-progress poster for the Phase 2 PrisMN study of budoprutug.

When and where is Climb Bio presenting CLYM116 data at ERA 2026?

Climb Bio will present CLYM116 data on June 5, 2026, from 15:03-15:09 BST in Focused Oral Room 2 at ERA 2026. According to the company, this talk covers extrapolation of PK and Ig suppression from nonhuman primates to healthy volunteers and initial Phase 1 data.

What is CLYM116 in Climb Bio’s pipeline for IgA nephropathy (IgAN)?

CLYM116 is described as a novel ‘sweeper’ anti-APRIL monoclonal antibody being developed for IgA nephropathy. According to Climb Bio, ERA 2026 presentations will show pharmacokinetic/pharmacodynamic modeling from nonhuman primates to humans and initial safety data from an ongoing Phase 1 study in healthy volunteers.

What is the PrisMN Phase 2 study of budoprutug in primary membranous nephropathy?

PrisMN is an ongoing Phase 2 study evaluating budoprutug, a low-fucosylated anti-CD19 monoclonal antibody, in primary membranous nephropathy. According to Climb Bio, a trial-in-progress poster will be presented June 4-5, 2026, in the Research Zone, Hall 4 (Ground Floor) at ERA 2026.

Where can investors find Climb Bio’s abstracts for ERA Congress 2026?

The CLYM116 and budoprutug abstracts are available on the ERA 2026 website. According to Climb Bio, abstract 780 covers the focused oral CLYM116 presentation and abstract 655 covers the PrisMN Phase 2 budoprutug poster in glomerular and tubulo-interstitial diseases sessions.