CLYMNASDAQHealthcare

Public company intelligence preview

CLIMB BIO INC

32 insider trades surfaced from the last year. This page shows only aggregate signals, not the underlying transactions, people, filings, filters, or AI workspace.

Snapshot

A narrow read on a much deeper workspace.

The preview gives search visitors enough signal to understand coverage. It does not expose transaction records, person-level profiles, filters, comparisons, or analyst workflows.

Insider trades, last 12 months
32
1 filed in the last 30 days
Acquisition / disposition count
22/10
Buy / Sell
Unique insiders active in the last year
12
Current insider positions tracked
21
20 active, 1 exited

Insider compensation

Public aggregate: $1.9M average total compensation across covered insiders.

Governance movement

Public aggregate: 4 governance events in the last year.

Institutional ownership

Public aggregate: 64 holders from the latest quarter.

Restricted sales and governance

Public counts, not the investigation layer.

The full product opens the underlying filings, insider context, historical holdings, comparison tools, and AI analysis.

Restricted-sale filings, 1Y
2
Restricted-sale insiders, 1Y
1
Planned sale shares, 1Y
150.0K
Planned sale value, 1Y
$874000.00
Insiders covered
6
Latest year: 2025
Personnel changes, 1Y
4
Board appointments, 1Y
4
Board departures, 1Y
4

Market context

Basic quote context for the preview.

Price
$10.66
Market cap
$552.6M
Volume
4,129.311
EPS
$-0.20
Revenue
$0.00
Employees
29

Company note

Context before the data.

Company Overview

Climb Bio Inc. is a Healthcare company in the Biotechnology industry that operates as a clinical-stage, pre-revenue developer of immune-mediated disease therapies. Its pipeline is centered on budoprutug, an anti-CD19 monoclonal antibody being studied in pMN, ITP, and SLE, and CLYM116, an anti-APRIL antibody for IgA nephropathy and related B-cell mediated diseases. The company has no approved products, no sales force, and no manufacturing infrastructure of its own, so it relies heavily on CROs, CDMOs, and licensing/collaboration partners. Its business model is therefore driven by clinical milestones, regulatory progress, and successful execution of partnered development programs rather than commercial sales.

Executive Compensation Practices

For a clinical-stage biotech like Climb Bio, executive compensation is typically tied to pipeline execution, capital preservation, and regulatory milestones rather than revenue growth. The filing summaries suggest that compensation metrics may emphasize progression of budoprutug and CLYM116 through clinical trials, initiation of new studies, successful regulatory interactions, and disciplined cash management given the company’s limited runway into 2027-2028. Because R&D and G&A are both rising as the organization expands, compensation packages may also include equity-based awards to attract and retain talent in a highly competitive Biotechnology labor market. Stock-based compensation is already material in G&A, which is common for companies in this sector that use equity incentives to align management with long-dated value creation and to conserve cash.

Insider Trading Considerations

Insider trading patterns at Climb Bio are likely to be closely influenced by clinical trial readouts, regulatory submissions, partnership activity, and financing needs, all of which can materially move the stock in Biotechnology. With no product revenue and a valuation tied almost entirely to pipeline success, insiders may be especially sensitive to blackout periods around trial updates, enrollment progress, and data releases for pMN, ITP, SLE, and CLYM116. The company’s ongoing cash burn, reliance on future capital, and use of an ATM program also make financing-related insider transactions important for researchers to watch, since equity raises can affect dilution and trading sentiment. In a Healthcare biotech setting, insiders may also trade cautiously around potentially material nonpublic information tied to trial design changes, manufacturing issues, or regulatory feedback from the FDA and foreign authorities.

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