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CGRP Monoclonal Antibody Therapy for Chronic Migraine in a Patient Refractory to Botox and Triple Oral Prophylaxis

From Daily, Disabling Headache to a 68% Reduction in Migraine Days

PATIENT PROFILE

Field

Details

Age

38 years

Gender

Female

Occupation

Marketing Manager, Private Sector

City

Bangalore

Presenting Complaint

Headache on 22 days per month, throbbing and disabling, with photophobia, phonophobia, and touch sensitivity of the scalp, present for six years and worsening over the last two

Diagnosis

Chronic Migraine, refractory to OnabotulinumtoxinA and triple oral prophylaxis, with a history of probable medication-overuse headache

Duration of Issue

Chronic (15+ headache days/month) for approximately 4 years, migraine history of 6 years

Previous Treatments

Topiramate, propranolol, and amitriptyline sequentially at adequate doses; three cycles of OnabotulinumtoxinA (Botox) via the PREEMPT protocol; frequent triptan and NSAID use for acute attacks

Date of Procedure

First CGRP monoclonal antibody injection: March 2026

Outcome

Excellent: sustained reduction in headache frequency and severity, return to full daily functioning

THE PROBLEM

Condition

The patient had a long-standing history of episodic migraine that gradually transformed into chronic migraine over several years, eventually reaching 22 headache days a month by the time she was referred to Dr. Guruprasad Hosurkar, a neurologist in Bangalore with a dedicated headache and migraine practice. Attacks were throbbing, one-sided more often than not, and accompanied by nausea, light and sound sensitivity, and scalp tenderness that made even brushing her hair painful on bad days.

She had already completed adequate, well-tolerated trials of three separate oral preventive medication classes: topiramate, propranolol, and amitriptyline, each given for at least eight weeks at an effective dose, without meaningful reduction in headache frequency. Three cycles of OnabotulinumtoxinA using the standard PREEMPT injection protocol, given twelve weeks apart, produced only a marginal, short-lived improvement. Frequent use of triptans and NSAIDs to manage acute attacks had, over time, added a component of medication-overuse headache, further complicating the clinical picture.

Emotional and Psychological Impact

By the time of referral, the patient had used the majority of her paid leave on headache days and had begun avoiding client-facing meetings she could not reliably guarantee attending. She described a persistent low-grade anxiety about the next attack, and a sense that she had already tried everything reasonable without result. The initial consultation focused on validating that her migraine was genuinely treatment-refractory by standard definitions, not a sign that nothing further could be done, and on introducing CGRP monoclonal antibody therapy as a distinct mechanism from everything she had tried so far.

CONSULTATION & TREATMENT PLAN

What Was Assessed

  • Detailed headache diary over four weeks: frequency, duration, severity, and associated features
  • MIDAS (Migraine Disability Assessment) and HIT-6 (Headache Impact Test) scoring
  • Screening for medication-overuse headache and acute medication use patterns
  • Review of prior preventive trials for adequacy of dose and duration
  • Neurological examination to exclude focal deficits
  • MRI brain to exclude secondary causes of chronic daily headache
  • Cardiovascular risk assessment prior to CGRP pathway blockade
  • Sleep, mood, and lifestyle trigger review

Why This Approach Was Chosen

Her chronic migraine met accepted criteria for treatment-refractory disease: inadequate response to three appropriately dosed oral preventive classes and to OnabotulinumtoxinA. This is the specific population in which CGRP monoclonal antibody therapy has the strongest evidence base, since it targets the calcitonin gene-related peptide pathway through a mechanism distinct from both her prior oral preventives and Botox. Addressing the medication-overuse component in parallel was essential, since overuse of acute medication can blunt the benefit of any preventive therapy if left unmanaged.

“When a patient has genuinely failed three well-chosen oral preventives and a full course of Botox, that is not the end of the road, it usually means we need a therapy that works through a different pathway altogether. CGRP monoclonal antibodies target the mechanism directly, and in appropriately refractory patients the response can be dramatic and rapid.” — Dr. Guruprasad Hosurkar. Full details on our Headache and Migraine Treatment blog.

BASELINE CLINICAL ASSESSMENT

Baseline monthly headache days: 22, of which the majority were moderate-to-severe in intensity with clear migrainous features. HIT-6 score: 68 (severe impact on daily functioning). MIDAS score: 45 (severe disability, equivalent to 45 lost or reduced-productivity days over the prior three months). Neurological examination was normal. MRI brain showed no structural abnormality. Acute medication use was averaging 18 days a month between triptans and NSAIDs combined, confirming probable medication-overuse headache alongside the chronic migraine.

TREATMENT DETAILS

Step-by-Step Overview

  • Structured, gradual withdrawal plan for overused acute medications, with a short bridging protocol to manage rebound symptoms
  • Loading dose of a CGRP monoclonal antibody, followed by monthly maintenance subcutaneous injections
  • Patient education and training for self-administered injection at home
  • Continued headache diary tracking throughout the first three months
  • Monthly clinical review for the first three months, then bimonthly
  • MIDAS and HIT-6 rescoring at 3 months and 6 months
  • Lifestyle and trigger-management counselling: sleep regularity, hydration, and meal timing

Treatment Facts

Field

Details

Duration

Ongoing: monthly injections with response reassessment at 3 and 6 months

Setting

Outpatient: KIMS Hospital, Mahadevapura, Bangalore; injections self-administered at home after initial training

Therapy

CGRP Monoclonal Antibody, monthly subcutaneous injection

Adjunct Management

Structured withdrawal of overused acute medication, trigger and lifestyle counselling

Complications

None; mild, transient injection-site redness after the first two doses

Inpatient Admission

Not required

POST-TREATMENT RESULTS

Headache frequency began declining within the first month, ahead of what is typically expected, alongside successful withdrawal from the overused acute medications. By three months, monthly headache days had fallen from 22 to 7, a 68% reduction, and the headaches that did occur were shorter and less severe. HIT-6 score improved from 68 to 46, and MIDAS score improved from 45 to 12, both reflecting a shift from severe to mild-moderate disability.

At six months, the reduction in headache frequency had been sustained, acute medication use had normalised to well within safe limits, and the patient had returned to a full client-facing workload without needing to plan around anticipated headache days.

Outcomes at a Glance

Field

Details

Headache-Day Reduction

✔ Monthly headache days: 22 to 7 at 3 months (68% reduction)

Disability Scores

✔ HIT-6: 68 to 46; MIDAS: 45 to 12

Medication-Overuse Resolved

✔ Acute medication use normalised to within safe limits

Functional Independence

✔ Returned to full client-facing work schedule

Patient Satisfaction

✔ Described the change as life-altering after years of daily anticipatory anxiety

Complications

✔ None significant

PATIENT FEEDBACK

Google Review
★★★★★
5.0

“I had tried three different daily tablets and three rounds of Botox before I met Dr. Hosurkar, and I genuinely thought I had run out of options. He explained clearly why a different type of injection could still work even though the others had not. Within two months my headache days had dropped by more than half, and I have not had to cancel a client meeting because of a migraine since.”

- Profile: Female · 38 years · Marketing Manager · Bangalore
- Condition: Chronic Migraine, refractory to Botox and triple oral prophylaxis, symptomatic for approximately 6 years
- Neurologist: Dr. Guruprasad Hosurkar | KIMS Hospital, Mahadevapura, Bangalore | March 2026

POST TREATMENT CARE & RECOVERY

Instructions Given to Patient

  • Continue monthly CGRP monoclonal antibody injections as scheduled, even after improvement is felt
  • Maintain the headache diary to track frequency, severity, and any breakthrough triggers
  • Keep acute medication use within safe limits (fewer than 10 days per month) to avoid recurrence of medication-overuse headache
  • Maintain regular sleep, hydration, and meal timing as baseline trigger management
  • Report any new or unusual symptoms, including significant constipation or injection-site reactions
  • Follow-up HIT-6 and MIDAS rescoring at 6 and 12 months
  • Discuss long-term continuation versus dose-interval adjustment once sustained response is confirmed

Recovery Timeline

Field

Details

Week 1–2

Loading dose given; acute medication withdrawal begins with bridging support

Week 4

Early reduction in headache frequency noted; acute medication overuse resolving

Month 3

Monthly headache days down to 7; HIT-6 and MIDAS scores substantially improved

Month 3–6

Sustained response confirmed; return to full work schedule

Month 6

Disability scores stable in the mild range; long-term therapy plan confirmed

FAQs

1. What is refractory chronic migraine?

Chronic migraine (15 or more headache days a month, with at least 8 having migraine features) is considered refractory when it fails to respond adequately to at least three classes of oral preventive medication and OnabotulinumtoxinA (Botox) given at adequate doses for an adequate duration.

2. What is CGRP monoclonal antibody therapy?

CGRP monoclonal antibodies are injectable preventive migraine medications that block the calcitonin gene-related peptide pathway involved in migraine attacks. They are given as a monthly or quarterly subcutaneous injection.

3. How is CGRP therapy different from Botox for chronic migraine?

Botox is injected into specific head and neck muscles every 12 weeks and works partly through peripheral nerve pathways, while CGRP monoclonal antibodies are given as a simple subcutaneous injection and act directly on the CGRP pathway believed to drive migraine attacks. The two mechanisms are different, so some patients who do not respond to Botox still respond to CGRP therapy.

4. How effective is CGRP monoclonal antibody therapy for chronic migraine?

In patients who have failed multiple prior preventive treatments, CGRP monoclonal antibodies commonly reduce monthly headache days by 50% or more within the first three months, with many patients seeing continued improvement over time.

5. What are the side effects of CGRP monoclonal antibody injections?

The most common side effects are mild injection-site reactions and occasional constipation. Serious side effects are uncommon, and the medications do not carry the sedation or cognitive side effects associated with many older oral preventives.

Disclaimer: This case study is for educational purposes only. Patient identity has been withheld per confidentiality guidelines. For related recovery stories, see our Essential Tremor DBS case study and our Young-Onset Parkinson’s STN-DBS case study, or browse more patient stories on our Case Study and Blog pages.

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