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Signal8 MCP Server

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Get Clinical Trials

get_clinical_trials
Read-only

Retrieve clinical trial data for a biotech or pharmaceutical company, including phase, status, conditions, and interventions, to analyze pipeline progress and catalyst events.

Instructions

Get clinical trial data for a biotech/pharma company including trial phase, status, conditions, and interventions. Use when analyzing a biotech company's pipeline or upcoming catalyst events.

Input Schema

TableJSON Schema
NameRequiredDescriptionDefault
limitNoMaximum number of clinical trials to return (1-50). Defaults to 10.
tickerYesStock ticker symbol (e.g., "MRNA", "PFE")

Output Schema

TableJSON Schema
NameRequiredDescriptionDefault
dataNo
Behavior3/5

Does the description disclose side effects, auth requirements, rate limits, or destructive behavior?

The description is consistent with the readOnlyHint annotation, indicating a read-only operation. It adds some detail about the data returned but does not cover all behavioral aspects like pagination or rate limits.

Agents need to know what a tool does to the world before calling it. Descriptions should go beyond structured annotations to explain consequences.

Conciseness5/5

Is the description appropriately sized, front-loaded, and free of redundancy?

Two sentences, front-loaded with the purpose, no unnecessary words. Every sentence serves a function.

Shorter descriptions cost fewer tokens and are easier for agents to parse. Every sentence should earn its place.

Completeness4/5

Given the tool's complexity, does the description cover enough for an agent to succeed on first attempt?

The description mentions the key data fields (phase, status, conditions, interventions) and the context of use. With an output schema available, this is largely complete, though it could mention the limit parameter's effect.

Complex tools with many parameters or behaviors need more documentation. Simple tools need less. This dimension scales expectations accordingly.

Parameters3/5

Does the description clarify parameter syntax, constraints, interactions, or defaults beyond what the schema provides?

Schema description coverage is 100%, so the input schema already documents both parameters. The description does not add additional parameter semantics beyond what the schema provides.

Input schemas describe structure but not intent. Descriptions should explain non-obvious parameter relationships and valid value ranges.

Purpose4/5

Does the description clearly state what the tool does and how it differs from similar tools?

The description clearly states it retrieves clinical trial data for a biotech/pharma company, specifying the included data types. However, it does not differentiate from the sibling tool 'search_clinical_trials', which might have a broader scope.

Agents choose between tools based on descriptions. A clear purpose with a specific verb and resource helps agents select the right tool.

Usage Guidelines3/5

Does the description explain when to use this tool, when not to, or what alternatives exist?

Provides a context for use ('when analyzing a biotech company's pipeline or upcoming catalyst events'), but does not mention when not to use or alternatives like 'search_clinical_trials'.

Agents often have multiple tools that could apply. Explicit usage guidance like "use X instead of Y when Z" prevents misuse.

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