CGRP Monoclonal Antibody Therapy for Chronic Migraine in a Patient Refractory to Botox and Triple Oral Prophylaxis
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
“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?
2. What is CGRP monoclonal antibody therapy?
3. How is CGRP therapy different from Botox for chronic migraine?
4. How effective is CGRP monoclonal antibody therapy for chronic migraine?
5. What are the side effects of CGRP monoclonal antibody injections?
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.
