Clinical Trial Endpoint Classifier β 4B (Qwen3.5-4B LoRA) β Best
The best performing endpoint classification model. A fine-tuned LoRA adapter on Qwen3.5-4B for extracting and classifying clinical trial endpoints from outcome text. Returns structured JSON with standardized endpoint names, measurement types, methods, and more.
Output Format
{
"endpoints": [
{
"endpoint_name_standardized": "Objective Response Rate",
"measurement_of": "tumor response",
"measurement_type": "binary",
"metric_type": "proportion",
"timeframe": "Week 24",
"measurement_method": "RECIST v1.1",
"evaluation_criteria": "CR or PR",
"unit": "%",
"population": null,
"is_composite": false,
"components": []
}
]
}
Field Definitions
| Field | Description | Examples |
|---|---|---|
endpoint_name_standardized |
Standardized endpoint name | "Overall Survival", "HbA1c", "PASI 75 Response Rate" |
measurement_of |
What is being measured | "tumor response", "glycated hemoglobin" |
measurement_type |
Type of measurement | continuous, binary, ordinal, time-to-event |
metric_type |
Statistical metric | mean, proportion, hazard ratio, change from baseline |
timeframe |
When measurement occurs | "Week 12", "Up to 36 months" |
measurement_method |
How it is measured | "blood test", "RECIST v1.1", "12-lead ECG" |
evaluation_criteria |
Criteria for evaluation | "PASI 75", "CR or PR" |
unit |
Unit of measurement | "%", "mg/dL", "mm" |
population |
Specific population | "adults aged 18-65" |
is_composite |
Whether composite endpoint | true / false |
components |
Components if composite | ["blood pressure", "heart rate"] |
Supports multiple endpoints from a single text (e.g., safety texts with 10+ sub-endpoints).
Training Details
| Base model | Qwen/Qwen3.5-4B |
| Method | LoRA (bf16, rank 16, alpha 16) |
| Training data | 1,948 samples (3,607 endpoints, 365 multi-endpoint texts) |
| Epochs | 3 |
| Final loss | 0.485 |
| Training time | 83 min on RTX 4090 |
| Framework | Unsloth + TRL SFTTrainer |
Hyperparameters
Method: LoRA (bf16, NOT 4-bit)
LoRA rank: 16, alpha: 16
Learning rate: 2e-4 (cosine)
Batch size: 2 (gradient accumulation 8, effective 16)
Epochs: 3
Optimizer: adamw_8bit
Sequence length: 2048
Gradient checkpointing: unsloth
Usage
import json
from unsloth import FastLanguageModel
from transformers import AutoTokenizer
import torch
model, tokenizer = FastLanguageModel.from_pretrained(
model_name="Shubh-0789/endpoint-qwen3.5-4b-lora",
max_seq_length=2048,
load_in_4bit=False,
load_in_16bit=True,
dtype=torch.bfloat16,
)
text_tokenizer = AutoTokenizer.from_pretrained("Shubh-0789/endpoint-qwen3.5-4b-lora")
FastLanguageModel.for_inference(model)
model.generation_config.pad_token_id = text_tokenizer.pad_token_id
clinical_text = "Primary endpoints are ORR and progression-free survival (PFS) assessed by RECIST v1.1 | [Time Frame: Up to 24 months]"
messages = [
{"role": "user", "content": f"Extract and classify the clinical trial endpoint from the following text. Return ONLY a JSON.\nText: {clinical_text}"}
]
inputs = text_tokenizer.apply_chat_template(
messages, tokenize=True, add_generation_prompt=True,
return_tensors="pt", return_dict=True,
).to(model.device)
with torch.no_grad():
outputs = model.generate(**inputs, max_new_tokens=512, temperature=0.1, do_sample=True)
result = text_tokenizer.decode(outputs[0][inputs["input_ids"].shape[1]:], skip_special_tokens=True)
endpoints = json.loads(result)
print(json.dumps(endpoints, indent=2))
Output:
{
"endpoints": [
{
"endpoint_name_standardized": "Objective Response Rate",
"measurement_of": "tumor response",
"measurement_type": "binary",
"metric_type": "proportion",
"timeframe": "Up to 24 months",
"measurement_method": "RECIST v1.1",
"evaluation_criteria": null,
"unit": "%",
"population": null,
"is_composite": false,
"components": []
},
{
"endpoint_name_standardized": "Progression-Free Survival",
"measurement_of": "disease progression or death",
"measurement_type": "time-to-event",
"metric_type": "hazard ratio",
"timeframe": "Up to 24 months",
"measurement_method": "RECIST v1.1",
"evaluation_criteria": null,
"unit": null,
"population": null,
"is_composite": false,
"components": []
}
]
}
With PEFT/Transformers
from peft import PeftModel
from transformers import AutoModelForCausalLM, AutoTokenizer
base_model = AutoModelForCausalLM.from_pretrained("Qwen/Qwen3.5-4B", torch_dtype="bfloat16", device_map="auto")
model = PeftModel.from_pretrained(base_model, "Shubh-0789/endpoint-qwen3.5-4b-lora")
tokenizer = AutoTokenizer.from_pretrained("Shubh-0789/endpoint-qwen3.5-4b-lora")
Model Comparison
| Model | Parameters | Loss | VRAM | Speed | Link |
|---|---|---|---|---|---|
| 0.8B | 856M | 0.617 | 3 GB | Fast | 0.8B |
| 4B | 4.6B | 0.485 | 10 GB | Moderate | This model (Best) |
Limitations
- Trained on English clinical trial text only
- Complex composite endpoints may need verification
- Minimum inference: any GPU with 10GB+ VRAM
Citation
@misc{endpoint-qwen3.5-4b-lora,
author = {Shubh-0789},
title = {Clinical Trial Endpoint Classifier β 4B (Qwen3.5-4B LoRA)},
year = {2026},
publisher = {Hugging Face},
url = {https://huggingface.co/Shubh-0789/endpoint-qwen3.5-4b-lora}
}