# Calcitonin gene-related peptide monoclonal antibody treatment for new daily persistent headache

**Authors:** Sanjay Cheema, Khadija Rerhou Rantell, Rachel Pickering, Susie Lagrata, Salwa Kamourieh, Manjit Matharu

PMC · DOI: 10.1186/s10194-025-02111-2 · The Journal of Headache and Pain · 2025-07-28

## TL;DR

This study found that calcitonin gene-related peptide monoclonal antibodies help about 25% of patients with new daily persistent headache, but are less effective than in chronic migraine.

## Contribution

First assessment of CGRP mAbs in NDPH, comparing their efficacy to chronic migraine and revealing lower effectiveness.

## Key findings

- 23% of NDPH patients had ≥30% improvement in headache days, compared to 46% in daily-CM and 84% in non-daily-CM.
- Only 11% of NDPH patients had ≥30% improvement in monthly headache days, suggesting limited effectiveness.
- CGRP mAbs were less effective in NDPH than in chronic migraine, indicating a need for new treatments.

## Abstract

New daily persistent headache (NDPH) is a rare headache disorder that often resembles chronic migraine (CM) phenotypically, but unlike CM is daily from onset. Several calcitonin gene-related peptide monoclonal antibodies (CGRP mAbs) have been proven to be effective in CM. It is not known whether CGRP mAbs are effective in NDPH. We sought to assess the efficacy, tolerability, and safety of CGRP mAbs in NDPH and compare their effect in NDPH to CM.

We performed an observational study using prospectively collected data in consecutive patients treated with CGRP mAbs in three groups: Group 1 included patients with NDPH with migraine features; Group 2 included patients with CM with daily headache; and Group 3 patients with non-daily CM. Given the observational nature of the study, propensity score matching was used in an attempt to balance the three groups on baseline factors to make them comparable. The majority of patients were treated with erenumab while the remainder received galcanezumab. Patients completed a headache diary and disability questionnaires at baseline and 12-week follow-up, with the primary endpoint being the proportion who achieved a reduction of at least 30% in monthly moderate-to-severe headache days (MSHD) compared between the three groups.

A total of 48 patients with NDPH, 101 with daily-CM, and 68 with non-daily-CM were included. From baseline to week 12, 11/47 (23%) of patients with NDPH had a ≥ 30% improvement in MSHD, compared to 46/99 (46%) in daily CM (OR 2.02, 95% CI 0.82–4.97, p = 0.125), and 51/61 (84%) in non-daily-CM (OR 4.41, 95% CI 1.17–16.6, p = 0.028). Only 5/47 (11%) of patients with NDPH had a ≥ 30% improvement in monthly headache days, and 24/44 (54%) reported an overall subjective improvement of ≥ 30%. Almost 50% of patients experienced at least one side effect, which were mild in almost all cases, and similar between groups.

CGRP mAbs were effective in approximately 1/4 patients with treatment-refractory NDPH,but less likely to be effective in NDPH than CM. This suggests that NDPH cannot be seen as equivalent to CM and that new treatment options are required for this highly disabling disorder.

## Full-text entities

- **Genes:** CALCA (calcitonin related polypeptide alpha) [NCBI Gene 796] {aka CALC1, CGRP, CGRP-I, CGRP-alpha, CGRP1, CT}
- **Diseases:** NDPH (MESH:D020773), headache (MESH:D006261), CM (MESH:D008881)
- **Chemicals:** galcanezumab (MESH:C000628360), erenumab (MESH:C000605816)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

3 references — full list in the complete paper: https://tomesphere.com/paper/PMC12306023/full.md

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Source: https://tomesphere.com/paper/PMC12306023